Simple Question (Direct)
Simple Question
Q286987
P688
Q181394
USER
What is the nutrient encoded by ABCA1 ?
(Q286987,P688,c(Q181394))
action filter_type
action find
entity Q286987
relation P688
type Q181394
['Q286987', 'P688', {'concept': 'Q181394'}]
SELECT DISTINCT ?x WHERE { resource:Q286987 property:P688 ?x . ?x rdf:type ontology:Q181394 }
ABCA1
action filter_type
action find
entity ABCA1
relation encodes
type nutrient
['ABCA1', 'encodes', {'concept': 'nutrient'}]
SELECT DISTINCT ?x WHERE { resource:ABCA1 property:encodes ?x . ?x rdf:type ontology:nutrient }
[]
nutrient
Q21115210
SYSTEM
ATP-binding cassette sub-family A member 1
Q21115210
(Q286987,P688,c(Q181394))
action filter_type
action find
entity Q286987
relation P688
type Q181394
The nutrient encoded by ABCA1 is the [ANSWER]
['Q286987', 'P688', {'concept': 'Q181394'}]
SELECT DISTINCT ?x WHERE { resource:Q286987 property:P688 ?x . ?x rdf:type ontology:Q181394 }
ATP-binding cassette sub-family A member 1
The nutrient encoded by ABCA1 is the ATP-binding cassette sub-family A member 1
ATP-binding cassette sub-family A member 1
action filter_type
action find
entity ABCA1
relation encodes
type nutrient
['ABCA1', 'encodes', {'concept': 'nutrient'}]
SELECT DISTINCT ?x WHERE { resource:ABCA1 property:encodes ?x . ?x rdf:type ontology:nutrient }
[]
Simple Question (Direct)
Simple Question|Single Entity
Q286987
P684
Q863908
USER
What is an otrhologus gene for ABCA1 ?
(Q286987,P684,c(Q863908))
action filter_type
action find
entity Q286987
relation P684
type Q863908
['Q286987', 'P684', {'concept': 'Q863908'}]
SELECT DISTINCT ?y WHERE { resource:Q286987 property:P684 ?y . ?y rdf:type ontology:Q863908 }
ABCA1
action filter_type
action find
entity ABCA1
relation ortholog
type nucleic acid sequence
['ABCA1', 'ortholog', {'concept': 'nucleic acid sequence'}]
SELECT DISTINCT ?y WHERE { resource:ABCA1 property:ortholog ?y . ?y rdf:type ontology:nucleic_acid_sequence }
[]
nucleic acid sequence
Q21129518
SYSTEM
Abca1
Q21129518
(Q286987,P684,c(Q863908))
action filter_type
action find
entity Q286987
relation P684
type Q863908
An otrhologus gene for ABCA1 is the [ANSWER]
['Q286987', 'P684', {'concept': 'Q863908'}]
SELECT DISTINCT ?y WHERE { resource:Q286987 property:P684 ?y . ?y rdf:type ontology:Q863908 }
Abca1
An otrhologus gene for ABCA1 is the Abca1
Abca1
action filter_type
action find
entity ABCA1
relation ortholog
type nucleic acid sequence
['ABCA1', 'ortholog', {'concept': 'nucleic acid sequence'}]
SELECT DISTINCT ?y WHERE { resource:ABCA1 property:ortholog ?y . ?y rdf:type ontology:nucleic_acid_sequence }
[]
Simple Question (Direct)
Simple Question|Single Entity
Q21115210
P703
Q16521
USER
Which taxon is ATP-binding cassette sub-family A member 1 found in ?
(Q21115210,P703,c(Q16521))
action filter_type
action find
entity Q21115210
relation P703
type Q16521
['Q21115210', 'P703', {'concept': 'Q16521'}]
SELECT DISTINCT ?d WHERE { resource:Q21115210 property:P703 ?d . ?d rdf:type ontology:Q16521 }
ATP-binding cassette sub-family A member 1
action filter_type
action find
entity ATP-binding cassette sub-family A member 1
relation found in taxon
type taxon
['ATP-binding cassette sub-family A member 1', 'found in taxon', {'concept': 'taxon'}]
SELECT DISTINCT ?d WHERE { resource:ATP-binding_cassette_sub-family_A_member_1 property:found_in_taxon ?d . ?d rdf:type ontology:taxon }
[]
taxon
Q15978631
SYSTEM
Homo sapiens
Q15978631
(Q21115210,P703,c(Q16521))
action filter_type
action find
entity Q21115210
relation P703
type Q16521
[ANSWER] is ATP-binding cassette sub-family A member 1 found in
['Q21115210', 'P703', {'concept': 'Q16521'}]
SELECT DISTINCT ?d WHERE { resource:Q21115210 property:P703 ?d . ?d rdf:type ontology:Q16521 }
Homo sapiens
Homo sapiens is ATP-binding cassette sub-family A member 1 found in
Homo sapiens
action filter_type
action find
entity ATP-binding cassette sub-family A member 1
relation found in taxon
type taxon
['ATP-binding cassette sub-family A member 1', 'found in taxon', {'concept': 'taxon'}]
SELECT DISTINCT ?d WHERE { resource:ATP-binding_cassette_sub-family_A_member_1 property:found_in_taxon ?d . ?d rdf:type ontology:taxon }
[]
Quantitative Reasoning (All)
Quantitative|Min/Max|Mult. entity type
P129
Q79529 Q181394 Q181394
USER
Which nutrients communicates with max number of chemical substances or nutrients ?
(c(Q181394),P129,c(Q79529)|c(Q181394))
action argmax
action union
action find_tuple_counts
relation P129
type Q181394
type Q79529
action find_tuple_counts
relation P129
type Q181394
type Q181394
[{'concept': 'Q181394'}, 'P129', [{'concept': 'Q79529'}, {'concept': 'Q181394'}]]
SELECT DISTINCT ?u WHERE { { SELECT DISTINCT ( MAX ( ?y ) AS ?m ) { SELECT DISTINCT ( COUNT ( ?r ) AS ?y ) ?d WHERE { ?r rdf:type ?q . VALUES ( ?q ) { ( ontology:Q79529 ) ( ontology:Q181394 ) } } GROUP BY ?d } } . { SELECT DISTINCT ( COUNT ( ?x ) AS ?l ) ?u WHERE { { ?u property:P129 ?x . ?u rdf:type ontology:Q181394 . ?x rdf:type ontology:Q79529 } UNION { ?u property:P129 ?x . ?u rdf:type ontology:Q181394 . ?x rdf:type ontology:Q181394 } } GROUP BY ?u } . FILTER ( ?l = ?m ) }
action argmax
action union
action find_tuple_counts
relation physically interacts with
type nutrient
type chemical substance
action find_tuple_counts
relation physically interacts with
type nutrient
type nutrient
[{'concept': 'nutrient'}, 'physically interacts with', [{'concept': 'chemical substance'}, {'concept': 'nutrient'}]]
SELECT DISTINCT ?u WHERE { { SELECT DISTINCT ( MAX ( ?y ) AS ?m ) { SELECT DISTINCT ( COUNT ( ?r ) AS ?y ) ?d WHERE { ?r rdf:type ?q . VALUES ( ?q ) { ( ontology:chemical_substance ) ( ontology:nutrient ) } } GROUP BY ?d } } . { SELECT DISTINCT ( COUNT ( ?x ) AS ?l ) ?u WHERE { { ?u property:physically_interacts_with ?x . ?u rdf:type ontology:nutrient . ?x rdf:type ontology:chemical_substance } UNION { ?u property:physically_interacts_with ?x . ?u rdf:type ontology:nutrient . ?x rdf:type ontology:nutrient } } GROUP BY ?u } . FILTER ( ?l = ?m ) }
[]
chemical substance nutrient nutrient
Q4639596
SYSTEM
5-hydroxytryptamine receptor 2B
Q4639596
(c(Q181394),P129,c(Q79529)|c(Q181394))
action argmax
action union
action find_tuple_counts
relation P129
type Q181394
type Q79529
action find_tuple_counts
relation P129
type Q181394
type Q181394
Receptor [ANSWER] communicates with max number of chemical substances or nutrients
[{'concept': 'Q181394'}, 'P129', [{'concept': 'Q79529'}, {'concept': 'Q181394'}]]
SELECT DISTINCT ?u WHERE { { SELECT DISTINCT ( MAX ( ?y ) AS ?m ) { SELECT DISTINCT ( COUNT ( ?r ) AS ?y ) ?d WHERE { ?r rdf:type ?q . VALUES ( ?q ) { ( ontology:Q79529 ) ( ontology:Q181394 ) } } GROUP BY ?d } } . { SELECT DISTINCT ( COUNT ( ?x ) AS ?l ) ?u WHERE { { ?u property:P129 ?x . ?u rdf:type ontology:Q181394 . ?x rdf:type ontology:Q79529 } UNION { ?u property:P129 ?x . ?u rdf:type ontology:Q181394 . ?x rdf:type ontology:Q181394 } } GROUP BY ?u } . FILTER ( ?l = ?m ) }
5-hydroxytryptamine receptor 2B
Receptor 5-hydroxytryptamine receptor 2B communicates with max number of chemical substances or nutrients
5-hydroxytryptamine receptor 2B
action argmax
action union
action find_tuple_counts
relation physically interacts with
type nutrient
type chemical substance
action find_tuple_counts
relation physically interacts with
type nutrient
type nutrient
[{'concept': 'nutrient'}, 'physically interacts with', [{'concept': 'chemical substance'}, {'concept': 'nutrient'}]]
SELECT DISTINCT ?u WHERE { { SELECT DISTINCT ( MAX ( ?y ) AS ?m ) { SELECT DISTINCT ( COUNT ( ?r ) AS ?y ) ?d WHERE { ?r rdf:type ?q . VALUES ( ?q ) { ( ontology:chemical_substance ) ( ontology:nutrient ) } } GROUP BY ?d } } . { SELECT DISTINCT ( COUNT ( ?x ) AS ?l ) ?u WHERE { { ?u property:physically_interacts_with ?x . ?u rdf:type ontology:nutrient . ?x rdf:type ontology:chemical_substance } UNION { ?u property:physically_interacts_with ?x . ?u rdf:type ontology:nutrient . ?x rdf:type ontology:nutrient } } GROUP BY ?u } . FILTER ( ?l = ?m ) }
[]
Logical Reasoning (All)
Logical|Union|Single_Relation
Q18031585 Q286987
P2293
Q2057971
USER
Which health problems are genetically linked with ABCA1 or SLC22A2 ?
OR((c(Q2057971),P2293,Q286987), (c(Q2057971),P2293,Q18031585))
action filter_type
action union
action find_reverse
entity Q286987
relation P2293
action find_reverse
entity Q18031585
relation P2293
type Q2057971
{'OR': [[{'concept': 'Q2057971'}, 'P2293', 'Q286987'], [{'concept': 'Q2057971'}, 'P2293', 'Q18031585']]}
SELECT DISTINCT ?n WHERE { { VALUES ( ?i ) { ( resource:Q286987 ) ( resource:Q18031585 ) } . ?n property:P2293 ?i } . ?n rdf:type ontology:Q2057971 }
SLC22A2 ABCA1
action filter_type
action union
action find_reverse
entity ABCA1
relation genetic association
action find_reverse
entity SLC22A2
relation genetic association
type health problem
{'OR': [[{'concept': 'health problem'}, 'genetic association', 'ABCA1'], [{'concept': 'health problem'}, 'genetic association', 'SLC22A2']]}
SELECT DISTINCT ?n WHERE { { VALUES ( ?i ) { ( resource:ABCA1 ) ( resource:SLC22A2 ) } . ?n property:genetic_association ?i } . ?n rdf:type ontology:health_problem }
[]
health problem
Q168403 Q1476525 Q2351083 Q844935 Q1054718
SYSTEM
myopia, lipid metabolism disorder, disease of metabolism, coronary artery disease, kidney disease
Q168403 Q1476525 Q2351083 Q844935 Q1054718
OR((c(Q2057971),P2293,Q286987), (c(Q2057971),P2293,Q18031585))
action filter_type
action union
action find_reverse
entity Q286987
relation P2293
action find_reverse
entity Q18031585
relation P2293
type Q2057971
Disease [ANSWERS] are genetically linked with ABCA1 or SLC22A2
{'OR': [[{'concept': 'Q2057971'}, 'P2293', 'Q286987'], [{'concept': 'Q2057971'}, 'P2293', 'Q18031585']]}
SELECT DISTINCT ?n WHERE { { VALUES ( ?i ) { ( resource:Q286987 ) ( resource:Q18031585 ) } . ?n property:P2293 ?i } . ?n rdf:type ontology:Q2057971 }
myopia lipid metabolism disorder disease of metabolism coronary artery disease kidney disease
Disease myopia, lipid metabolism disorder, disease of metabolism, coronary artery disease and kidney disease are genetically linked with ABCA1 or SLC22A2
myopia lipid metabolism disorder disease of metabolism coronary artery disease kidney disease
action filter_type
action union
action find_reverse
entity ABCA1
relation genetic association
action find_reverse
entity SLC22A2
relation genetic association
type health problem
{'OR': [[{'concept': 'health problem'}, 'genetic association', 'ABCA1'], [{'concept': 'health problem'}, 'genetic association', 'SLC22A2']]}
SELECT DISTINCT ?n WHERE { { VALUES ( ?i ) { ( resource:ABCA1 ) ( resource:SLC22A2 ) } . ?n property:genetic_association ?i } . ?n rdf:type ontology:health_problem }
[]
Quantitative Reasoning (All)
Quantitative|Atleast/ Atmost/ Approx. the same/Equal|Mult. entity type
P780
Q1441305 Q12136 Q2057971
USER
Which health problems do the presence of approximately 6 medical signs and diseases indicate ?
(c(Q2057971),P780,c(Q1441305)|c(Q12136))
action approx
action union
action find_tuple_counts
relation P780
type Q2057971
type Q1441305
action find_tuple_counts
relation P780
type Q2057971
type Q12136
value 6
[{'concept': 'Q2057971'}, 'P780', [{'concept': 'Q1441305'}, {'concept': 'Q12136'}]]
SELECT DISTINCT ?d WHERE { { SELECT DISTINCT ( COUNT ( ?v ) AS ?k ) ?d WHERE { VALUES ( ?e ) { ( ontology:Q12136 ) ( ontology:Q1441305 ) } . ?v rdf:type ?e } GROUP BY ?d } . FILTER ( ?k = 6 ) }
action approx
action union
action find_tuple_counts
relation symptoms
type health problem
type medical sign
action find_tuple_counts
relation symptoms
type health problem
type disease
value 6
[{'concept': 'health problem'}, 'symptoms', [{'concept': 'medical sign'}, {'concept': 'disease'}]]
SELECT DISTINCT ?d WHERE { { SELECT DISTINCT ( COUNT ( ?v ) AS ?k ) ?d WHERE { VALUES ( ?e ) { ( ontology:disease ) ( ontology:medical_sign ) } . ?v rdf:type ?e } GROUP BY ?d } . FILTER ( ?k = 6 ) }
[]
medical sign disease health problem
Q131755 Q221668 Q47912
SYSTEM
bipolar disorder, acute cystitis, lung cancer
Q131755 Q30953 Q47912 Q221668 Q180664
(c(Q2057971),P780,c(Q1441305)|c(Q12136))
action approx
action union
action find_tuple_counts
relation P780
type Q2057971
type Q1441305
action find_tuple_counts
relation P780
type Q2057971
type Q12136
value 6
[ANSWERS] the presence of approximately 6 medical signs and diseases indicate
[{'concept': 'Q2057971'}, 'P780', [{'concept': 'Q1441305'}, {'concept': 'Q12136'}]]
SELECT DISTINCT ?d WHERE { { SELECT DISTINCT ( COUNT ( ?v ) AS ?k ) ?d WHERE { VALUES ( ?e ) { ( ontology:Q12136 ) ( ontology:Q1441305 ) } . ?v rdf:type ?e } GROUP BY ?d } . FILTER ( ?k = 6 ) }
bipolar disorder dengue fever lung cancer acute cystitis acute lymphocytic leukemia
Bipolar disorder, acute cystitis and lung cancer the presence of approximately 6 medical signs and diseases indicate
bipolar disorder acute cystitis lung cancer
action approx
action union
action find_tuple_counts
relation symptoms
type health problem
type medical sign
action find_tuple_counts
relation symptoms
type health problem
type disease
value 6
[{'concept': 'health problem'}, 'symptoms', [{'concept': 'medical sign'}, {'concept': 'disease'}]]
SELECT DISTINCT ?d WHERE { { SELECT DISTINCT ( COUNT ( ?v ) AS ?k ) ?d WHERE { VALUES ( ?e ) { ( ontology:disease ) ( ontology:medical_sign ) } . ?v rdf:type ?e } GROUP BY ?d } . FILTER ( ?k = 6 ) }
[]
Clarification
Comparative|More/Less|Mult. entity type|Indirect
P780
Q2057971 Q12136 Q2057971
USER
Which health problems are indicated by the existence of approximately the same number of health problems or diseases as that health problem ?
(c(Q2057971),P780,c(Q2057971)|c(Q12136))
[{'concept': 'Q2057971'}, 'P780', [{'concept': 'Q2057971'}, {'concept': 'Q12136'}]]
SELECT DISTINCT ?z WHERE { { { ?z property:P780 ?z } UNION { ?z property:P780 ?y } } . ?z rdf:type ontology:Q2057971 . ?y rdf:type ontology:Q12136 }
[{'concept': 'health problem'}, 'symptoms', [{'concept': 'health problem'}, {'concept': 'disease'}]]
SELECT DISTINCT ?z WHERE { { { ?z property:symptoms ?z } UNION { ?z property:symptoms ?y } } . ?z rdf:type ontology:health_problem . ?y rdf:type ontology:disease }
[]
health problem disease health problem
Comparative|More/Less|Mult. entity type|Clarification
Q221668
SYSTEM
Did you mean acute cystitis ?
(c(Q2057971),P780,c(Q2057971)|c(Q12136))
[ANSWER]
[{'concept': 'Q2057971'}, 'P780', [{'concept': 'Q2057971'}, {'concept': 'Q12136'}]]
SELECT DISTINCT ?z WHERE { { { ?z property:P780 ?z } UNION { ?z property:P780 ?y } } . ?z rdf:type ontology:Q2057971 . ?y rdf:type ontology:Q12136 }
Did you mean acute cystitis ?
acute cystitis
[{'concept': 'health problem'}, 'symptoms', [{'concept': 'health problem'}, {'concept': 'disease'}]]
SELECT DISTINCT ?z WHERE { { { ?z property:symptoms ?z } UNION { ?z property:symptoms ?y } } . ?z rdf:type ontology:health_problem . ?y rdf:type ontology:disease }
[]
Comparative Reasoning (All)
USER
No, I meant bipolar disorder. Could you tell me the answer for that?
(c(Q2057971),P780,c(Q2057971)|c(Q12136))
Q131755
[{'concept': 'Q2057971'}, 'P780', [{'concept': 'Q2057971'}, {'concept': 'Q12136'}]]
[{'concept': 'health problem'}, 'symptoms', [{'concept': 'health problem'}, {'concept': 'disease'}]]
[]
SYSTEM
17
Q2583514 Q7688951 Q2388598 Q39222 Q3508705 Q1198391 Q190564 Q10529545 Q127724 Q8071861 Q1077603 Q4421929 Q30953 Q212961 Q264118 Q1981276 Q432396
(c(Q2057971),P780,c(Q2057971)|c(Q12136))
[ANSWER]
[{'concept': 'Q2057971'}, 'P780', [{'concept': 'Q2057971'}, {'concept': 'Q12136'}]]
SELECT DISTINCT ?z WHERE { { { ?z property:P780 ?z } UNION { ?z property:P780 ?y } } . ?z rdf:type ontology:Q2057971 . ?y rdf:type ontology:Q12136 }
Argentine hemorrhagic fever Taussig–Bing syndrome Ollier disease rabies Timothy syndrome intracranial aneurysm Huntington's disease hyperandrogenism cataract Zika fever malignant mesothelioma Hippocampal sclerosis dengue fever pancreatic cancer acute myeloid leukemia neuroendocrine tumor achromatopsia
17
[{'concept': 'health problem'}, 'symptoms', [{'concept': 'health problem'}, {'concept': 'disease'}]]
SELECT DISTINCT ?z WHERE { { { ?z property:symptoms ?z } UNION { ?z property:symptoms ?y } } . ?z rdf:type ontology:health_problem . ?y rdf:type ontology:disease }
[]
Quantitative Reasoning (All)
Quantitative|Min/Max|Single entity type
P828
Q12136 Q2057971
USER
Which diseases are the causes of min number of health problems ?
(c(Q2057971),P828,Q205972)
action argmin
action find_reverse_tuple_counts
relation P828
type Q12136
type Q2057971
[{'concept': 'Q2057971'}, 'P828', 'Q205972']
SELECT DISTINCT ?f WHERE { { SELECT DISTINCT ( MIN ( ?a ) AS ?d ) { SELECT DISTINCT ?b ( COUNT ( ?s ) AS ?a ) WHERE { ?b rdf:type ontology:Q12136 . ?s rdf:type ontology:Q2057971 . ?s property:P828 ?b } GROUP BY ?b } } . { SELECT DISTINCT ?f ( COUNT ( ?m ) AS ?v ) WHERE { ?m property:P828 ?f . ?f rdf:type ontology:Q12136 . ?m rdf:type ontology:Q2057971 } GROUP BY ?f } . FILTER ( ?v = ?d ) }
action argmin
action find_reverse_tuple_counts
relation has cause
type disease
type health problem
[{'concept': 'health problem'}, 'has cause', 'drunkenness']
SELECT DISTINCT ?f WHERE { { SELECT DISTINCT ( MIN ( ?a ) AS ?d ) { SELECT DISTINCT ?b ( COUNT ( ?s ) AS ?a ) WHERE { ?b rdf:type ontology:disease . ?s rdf:type ontology:health_problem . ?s property:has_cause ?b } GROUP BY ?b } } . { SELECT DISTINCT ?f ( COUNT ( ?m ) AS ?v ) WHERE { ?m property:has_cause ?f . ?f rdf:type ontology:disease . ?m rdf:type ontology:health_problem } GROUP BY ?f } . FILTER ( ?v = ?d ) }
[]
disease health problem
Q189331 Q1942814 Q205972
SYSTEM
cardiac dysrhythmia, Foot drop, drunkenness
Q18377123 Q189331 Q33487 Q1942814 Q2866610 Q205972
(c(Q2057971),P828,Q205972)
action argmin
action find_reverse_tuple_counts
relation P828
type Q12136
type Q2057971
[ANSWERS] are the causes of min number of health problems
[{'concept': 'Q2057971'}, 'P828', 'Q205972']
SELECT DISTINCT ?f WHERE { { SELECT DISTINCT ( MIN ( ?a ) AS ?d ) { SELECT DISTINCT ?b ( COUNT ( ?s ) AS ?a ) WHERE { ?b rdf:type ontology:Q12136 . ?s rdf:type ontology:Q2057971 . ?s property:P828 ?b } GROUP BY ?b } } . { SELECT DISTINCT ?f ( COUNT ( ?m ) AS ?v ) WHERE { ?m property:P828 ?f . ?f rdf:type ontology:Q12136 . ?m rdf:type ontology:Q2057971 } GROUP BY ?f } . FILTER ( ?v = ?d ) }
iodine deficiency cardiac dysrhythmia homophobia Foot drop hyposalivation drunkenness
Cardiac dysrhythmia, Foot drop and drunkenness are the causes of min number of health problems
cardiac dysrhythmia Foot drop drunkenness
action argmin
action find_reverse_tuple_counts
relation has cause
type disease
type health problem
[{'concept': 'health problem'}, 'has cause', 'drunkenness']
SELECT DISTINCT ?f WHERE { { SELECT DISTINCT ( MIN ( ?a ) AS ?d ) { SELECT DISTINCT ?b ( COUNT ( ?s ) AS ?a ) WHERE { ?b rdf:type ontology:disease . ?s rdf:type ontology:health_problem . ?s property:has_cause ?b } GROUP BY ?b } } . { SELECT DISTINCT ?f ( COUNT ( ?m ) AS ?v ) WHERE { ?m property:has_cause ?f . ?f rdf:type ontology:disease . ?m rdf:type ontology:health_problem } GROUP BY ?f } . FILTER ( ?v = ?d ) }
[]
Logical Reasoning (All)
Logical|Union|Multiple_Relation
Q162606 Q286987
P2293 P1995
Q2057971
USER
Which health problems are genetically associated with ABCA1 or are known for endocrinology as the associated medical speciality ?
OR((c(Q2057971),P2293,Q286987), (c(Q2057971),P1995,Q162606))
action filter_type
action union
action find_reverse
entity Q286987
relation P2293
action find_reverse
entity Q162606
relation P1995
type Q2057971
{'OR': [[{'concept': 'Q2057971'}, 'P2293', 'Q286987'], [{'concept': 'Q2057971'}, 'P1995', 'Q162606']]}
SELECT DISTINCT ?f WHERE { { { ?f property:P2293 resource:Q286987 } UNION { ?f property:P1995 resource:Q162606 } } . ?f rdf:type ontology:Q2057971 }
endocrinology ABCA1
action filter_type
action union
action find_reverse
entity ABCA1
relation genetic association
action find_reverse
entity endocrinology
relation medical specialty
type health problem
{'OR': [[{'concept': 'health problem'}, 'genetic association', 'ABCA1'], [{'concept': 'health problem'}, 'medical specialty', 'endocrinology']]}
SELECT DISTINCT ?f WHERE { { { ?f property:genetic_association resource:ABCA1 } UNION { ?f property:medical_specialty resource:endocrinology } } . ?f rdf:type ontology:health_problem }
[]
health problem
Q117121 Q3441028 Q1054713 Q1474877 Q275385 Q1313510 Q187842 Q3281373 Q1747726 Q1573307
SYSTEM
Some of them are Wilson disease, Norum disease, xerophthalmia, Hypercalcaemia, variegate porphyria, Hypophosphatasia, autoimmune thyroiditis, metal metabolism disorder, tyrosinemia type I, Wernicke encephalopathy
Q2349546 Q8041557 Q4826993 Q15051322 Q567820 Q3273331 Q271759 Q275385 Q1263039 Q1053120 Q3622611 Q774483 Q6013981 Q1507609 Q675311 Q1598200 Q928424 Q1396345 Q2622714 Q3281373 Q1140000 Q16501 Q1821559 Q1640860 Q922411 Q1538213 Q994859 Q4358039 Q1313510 Q1585743 Q7843329 Q1327712 Q16483 Q10264745 Q2831905 Q1515038 Q1506216 Q1573307 Q1553018 Q177878 Q4082071 Q12174 Q4198677 Q1165179 Q3704730 Q7254411 Q512313 Q1125675 Q2378552 Q183392 Q337604 Q1500373 Q1442621 Q4712685 Q1149042 Q1149046 Q200985 Q13581332 Q511372 Q1476965 Q213098 Q3338677 Q53829 Q219223 Q3043161 Q3100515 Q1529983 Q1947298 Q1433936 Q473262 Q218712 Q369262 Q750826 Q7263801 Q2046550 Q615645 Q17120992 Q787751 Q3242224 Q5437988 Q991538 Q5959735 Q390475 Q1365789 Q3278042 Q6673122 Q402575 Q424247 Q7136145 Q1939330 Q168403 Q1421738 Q187842 Q184084 Q1419931 Q1516083 Q11312280 Q1759389 Q1479497 Q877827 Q1479681 Q2661443 Q3281322 Q2309612 Q2351083 Q647630 Q4368173 Q3043147 Q501829 Q790971 Q213151 Q2019832 Q1207967 Q1474877 Q12412172 Q16499 Q823140 Q934034 Q3801524 Q1516012 Q1906054 Q500816 Q3025883 Q966229 Q339547 Q16944888 Q639203 Q1750471 Q319812 Q1747726 Q859142 Q7250337 Q7830387 Q8282 Q776026 Q1876206 Q3441028 Q3144934 Q1054713 Q494922 Q3508729 Q1753778 Q12167 Q1144618 Q3444851 Q762713 Q816798 Q3234995 Q3153671 Q7861692 Q799615 Q16495 Q1518637 Q2165266 Q657193 Q5282519 Q189580 Q2017741 Q167050 Q2349695 Q651680 Q5150905 Q2711291 Q1378921 Q2033861 Q224513 Q1154619 Q2500124 Q630090 Q1493513 Q1276885 Q16252204 Q1120682 Q1641171 Q1614115 Q13637039 Q669822 Q752216 Q1641384 Q4347774 Q117121 Q829150 Q5517825 Q506433 Q379418 Q1615557 Q6072985 Q366868 Q959457 Q7936970 Q1516888 Q1691351 Q531012 Q1122668 Q221441 Q7263794 Q6710283 Q477390 Q861645 Q727436 Q794086 Q11835644 Q49970 Q219102 Q163865 Q1609755 Q81867 Q844935 Q582904 Q165135 Q560337 Q1179460 Q819207 Q3540902 Q725845 Q3281227 Q5220984 Q17008739 Q1654860 Q675010 Q937818 Q654425 Q2246688 Q250449 Q1759600 Q1344835 Q5513690 Q5513691 Q1739759 Q742500 Q576109 Q194041 Q1476525 Q202758 Q4117241 Q2919083
OR((c(Q2057971),P2293,Q286987), (c(Q2057971),P1995,Q162606))
action filter_type
action union
action find_reverse
entity Q286987
relation P2293
action find_reverse
entity Q162606
relation P1995
type Q2057971
[ANSWERS] are genetically associated with ABCA1 or are known for endocrinology as the associated medical speciality
{'OR': [[{'concept': 'Q2057971'}, 'P2293', 'Q286987'], [{'concept': 'Q2057971'}, 'P1995', 'Q162606']]}
SELECT DISTINCT ?f WHERE { { { ?f property:P2293 resource:Q286987 } UNION { ?f property:P1995 resource:Q162606 } } . ?f rdf:type ontology:Q2057971 }
Canavan disease X-linked hypophosphatemic rickets autosomal dominant hypophosphatemic rickets Inborn error of lipid metabolism Alexander disease acatalasia porphyria variegate porphyria Dubin–Johnson syndrome Gitelman syndrome Secondary hyperparathyroidism Galactosemia carbohydrate metabolic disorder Ochronosis autoimmune polyendocrine syndrome metabolic acidosis Barth syndrome Farber lipogranulomatosis cholesteryl ester storage disease metal metabolism disorder Crigler-Najjar syndrome hypothyroidisms leukodystrophy hyperaldosteronism hypopituitarism lipodystrophy homocystinuria neuronal ceroid lipofuscinosis Hypophosphatasia urea cycle disorder triple-A syndrome alpha 1-antitrypsin deficiency toxic diffuse goiter biotin deficiency ocular albinism thyroid hormone resistance syndrome Hermansky-Pudlak syndrome Wernicke encephalopathy Multiple endocrine neoplasia Fucosidosis protein-energy malnutrition obesity complications of diabetes mellitus Kallmann syndrome adrenocorticotropic hormone deficiency pseudo-Hurler polydystrophy Androgen insensitivity syndrome Congenital disorder of glycosylation Hypoaldosteronism rickets aceruloplasminemia lactic acidosis Tangier disease Albright's hereditary osteodystrophy cystinosis cystinuria Hartnup disease familial visceral amyloidosis Krabbe disease xanthinuria progeria paramyloidosis Thyroid nodule lactose intolerance ornithine carbamoyltransferase deficiency hypervitaminosis A Hunter syndrome glycogen storage disease VI Hyperprolactinaemia Complete androgen insensitivity syndrome Zollinger-Ellison syndrome Growth hormone deficiency medium chain acyl-CoA dehydrogenase deficiency pyruvate decarboxylase deficiency diabetic neuropathy Fabry disease Hyperglycerolemia glycogen storage disease V congenital generalized lipodystrophy Fatty-acid metabolism disorder pituitary apoplexy hypolipoproteinemia bilirubin metabolic disorder glycogen storage disease II Isovaleric acidemia thyroid gland disease maple syrup urine disease acute intermittent porphyria parathyroid gland disease Conn's syndrome myopia glycogen storage disease autoimmune thyroiditis beriberi Niemann–Pick disease piebaldism pituitary-dependent Cushing's disease cutaneous porphyria Porphyria cutanea tarda diabetic ketoacidosis Mucopolysaccharidosis endocrine system disease peroxisomal disease sphingolipidosis disease of metabolism premature ovarian failure subacute thyroiditis fructose-1,6-bisphosphatase deficiency gigantism Bartter disease kwashiorkor glycoproteinosis renal glycosuria Hypercalcaemia Neurogenic diabetes insipidus hyperthyroidism Hereditary coproporphyria Chédiak–Higashi syndrome hyperpituitarism Delayed puberty mucopolysaccharidosis I polycystic ovary syndrome type 2 diabetes mellitus myxedema Carcinoid syndrome mineral deficiency Menkes disease Sly syndrome abetalipoproteinemia tyrosinemia type I Citrullinemia Propionic acidemia Plummer's disease Addison's disease biotinidase deficiency Pelizaeus-Merzbacher disease Norum disease hemochromatosis xerophthalmia glycogen storage disease III Occipital horn syndrome Batten disease malnutrition familial Mediterranean fever hypobetalipoproteinemia hypercholesterolemia amyloidosis vitamin B12 deficiency lysinuric protein intolerance tyrosinemia type III osteitis fibrosa Riedel's thyroiditis VIPoma Nelson syndrome metabolic syndrome calcium metabolism disease acromegaly oculocutaneous albinism Sertoli cell-only syndrome familial lipoprotein lipase deficiency alkaptonuria mixed hyperlipidemia familial hypercholesterolemia euthyroid sick syndrome carnitine palmitoyltransferase II deficiency Precocious puberty Werner syndrome Urbach–Wiethe disease glycogen storage disease I gangliosidosis Froelich syndrome dicarboxylic aminoaciduria metachromatic leukodystrophy hypervitaminosis D hypervolemia hyperlysinemia Laron syndrome Gilbert syndrome hypophosphatemia autoimmune polyendocrine syndrome type 1 Wilson disease glycogen storage disease IV Galactokinase deficiency Trimethylaminuria keratomalacia adiposis dolorosa iron metabolism disease congenital adrenal hyperplasia inappropriate ADH syndrome vitamin K deficiency hemorrhagic disease inclusion-cell disease lipomatosis congenital hypothyroidism tyrosinemia pellagra pyruvate carboxylase deficiency disease Lysosomal Acid Lipase Deficiency Hyperinsulinism Gaucher's disease Lesch-Nyhan syndrome hypokalemia thyroiditis hyperuricemia Cushing's syndrome scurvy hereditary fructose intolerance syndrome albino coronary artery disease marasmus goiter Tay–Sachs disease Fanconi syndrome Pseudohypoparathyroidism lipid storage disease histidinemia mucosulfatidosis Danon disease Latent Iron Deficiency Argininosuccinic aciduria lysosomal storage disease acrodermatitis enteropathica Waterhouse-Friderichsen syndrome pseudoporphyria alpha-mannosidosis erythropoietic protoporphyria hyperparathyroidism gangliosidosis GM1 gangliosidosis GM2 Keshan disease Methylmalonic acidemia Maroteaux–Lamy syndrome phenylketonuria lipid metabolism disorder hypoglycemia autoimmune polyendocrine syndrome type 2 primary hyperparathyroidism
Wilson disease, Norum disease, xerophthalmia, Hypercalcaemia, variegate porphyria, Hypophosphatasia, autoimmune thyroiditis, metal metabolism disorder, tyrosinemia type I and Wernicke encephalopathy are genetically associated with ABCA1 or are known for endocrinology as the associated medical speciality
Wilson disease Norum disease xerophthalmia Hypercalcaemia variegate porphyria Hypophosphatasia autoimmune thyroiditis metal metabolism disorder tyrosinemia type I Wernicke encephalopathy
action filter_type
action union
action find_reverse
entity ABCA1
relation genetic association
action find_reverse
entity endocrinology
relation medical specialty
type health problem
{'OR': [[{'concept': 'health problem'}, 'genetic association', 'ABCA1'], [{'concept': 'health problem'}, 'medical specialty', 'endocrinology']]}
SELECT DISTINCT ?f WHERE { { { ?f property:genetic_association resource:ABCA1 } UNION { ?f property:medical_specialty resource:endocrinology } } . ?f rdf:type ontology:health_problem }
[]