Simple Question (Direct)
Simple Question
Q21131625
P703
Q16521
USER
Where is Androglobin found ?
(Q21131625,P703,c(Q16521))
action filter_type
action find
entity Q21131625
relation P703
type Q16521
['Q21131625', 'P703', {'concept': 'Q16521'}]
SELECT DISTINCT ?y WHERE { resource:Q21131625 property:P703 ?y . ?y rdf:type ontology:Q16521 }
Androglobin
action filter_type
action find
entity Androglobin
relation found in taxon
type taxon
['Androglobin', 'found in taxon', {'concept': 'taxon'}]
SELECT DISTINCT ?y WHERE { resource:Androglobin property:found_in_taxon ?y . ?y rdf:type ontology:taxon }
[]
taxon
Q15978631
SYSTEM
Homo sapiens
Q15978631
(Q21131625,P703,c(Q16521))
action filter_type
action find
entity Q21131625
relation P703
type Q16521
Androglobin is found in [ANSWER]
['Q21131625', 'P703', {'concept': 'Q16521'}]
SELECT DISTINCT ?y WHERE { resource:Q21131625 property:P703 ?y . ?y rdf:type ontology:Q16521 }
Homo sapiens
Androglobin is found in Homo sapiens
Homo sapiens
action filter_type
action find
entity Androglobin
relation found in taxon
type taxon
['Androglobin', 'found in taxon', {'concept': 'taxon'}]
SELECT DISTINCT ?y WHERE { resource:Androglobin property:found_in_taxon ?y . ?y rdf:type ontology:taxon }
[]
Simple Question (Direct)
Simple Question|Single Entity
Q21131625
P702
Q863908
USER
Which nucleic acid sequence encodes Androglobin ?
(Q21131625,P702,c(Q863908))
action filter_type
action find
entity Q21131625
relation P702
type Q863908
['Q21131625', 'P702', {'concept': 'Q863908'}]
SELECT DISTINCT ?n WHERE { resource:Q21131625 property:P702 ?n . ?n rdf:type ontology:Q863908 }
Androglobin
action filter_type
action find
entity Androglobin
relation encoded by
type nucleic acid sequence
['Androglobin', 'encoded by', {'concept': 'nucleic acid sequence'}]
SELECT DISTINCT ?n WHERE { resource:Androglobin property:encoded_by ?n . ?n rdf:type ontology:nucleic_acid_sequence }
[]
nucleic acid sequence
Q18046320
SYSTEM
ADGB
Q18046320
(Q21131625,P702,c(Q863908))
action filter_type
action find
entity Q21131625
relation P702
type Q863908
[ANSWER] encodes Androglobin
['Q21131625', 'P702', {'concept': 'Q863908'}]
SELECT DISTINCT ?n WHERE { resource:Q21131625 property:P702 ?n . ?n rdf:type ontology:Q863908 }
ADGB
ADGB encodes Androglobin
ADGB
action filter_type
action find
entity Androglobin
relation encoded by
type nucleic acid sequence
['Androglobin', 'encoded by', {'concept': 'nucleic acid sequence'}]
SELECT DISTINCT ?n WHERE { resource:Androglobin property:encoded_by ?n . ?n rdf:type ontology:nucleic_acid_sequence }
[]
Simple Question (Coreferenced)
Simple Question|Single Entity|Indirect
Q18046320
P684
Q863908
USER
What is the name of the species that has that one as its orthologous gene ?
(c(Q863908),P684,Q18046320)
action filter_type
action find
entity Q18046320
relation P684
type Q863908
[{'concept': 'Q863908'}, 'P684', 'Q18046320']
SELECT DISTINCT ?i WHERE { resource:Q18046320 property:P684 ?i . ?i rdf:type ontology:Q863908 }
ADGB
action filter_type
action find
entity ADGB
relation ortholog
type nucleic acid sequence
[{'concept': 'nucleic acid sequence'}, 'ortholog', 'ADGB']
SELECT DISTINCT ?i WHERE { resource:ADGB property:ortholog ?i . ?i rdf:type ontology:nucleic_acid_sequence }
[]
nucleic acid sequence
Q18296658
SYSTEM
Adgb
Q18296658
(c(Q863908),P684,Q18046320)
action filter_type
action find
entity Q18046320
relation P684
type Q863908
The name of the species that has that one as its orthologous gene is the [ANSWER]
[{'concept': 'Q863908'}, 'P684', 'Q18046320']
SELECT DISTINCT ?i WHERE { resource:Q18046320 property:P684 ?i . ?i rdf:type ontology:Q863908 }
Adgb
The name of the species that has that one as its orthologous gene is the Adgb
Adgb
action filter_type
action find
entity ADGB
relation ortholog
type nucleic acid sequence
[{'concept': 'nucleic acid sequence'}, 'ortholog', 'ADGB']
SELECT DISTINCT ?i WHERE { resource:ADGB property:ortholog ?i . ?i rdf:type ontology:nucleic_acid_sequence }
[]
Simple Question (Direct)
Simple Question|Single Entity
Q18046320
P688
Q181394
USER
What is encoded by ADGB ?
(Q18046320,P688,c(Q181394))
action filter_type
action find
entity Q18046320
relation P688
type Q181394
['Q18046320', 'P688', {'concept': 'Q181394'}]
SELECT DISTINCT ?h WHERE { ?h rdf:type ontology:Q181394 . resource:Q18046320 property:P688 ?h }
ADGB
action filter_type
action find
entity ADGB
relation encodes
type nutrient
['ADGB', 'encodes', {'concept': 'nutrient'}]
SELECT DISTINCT ?h WHERE { ?h rdf:type ontology:nutrient . resource:ADGB property:encodes ?h }
[]
nutrient
Q21131625
SYSTEM
Androglobin
Q21131625
(Q18046320,P688,c(Q181394))
action filter_type
action find
entity Q18046320
relation P688
type Q181394
[ANSWER] is encoded by ADGB
['Q18046320', 'P688', {'concept': 'Q181394'}]
SELECT DISTINCT ?h WHERE { ?h rdf:type ontology:Q181394 . resource:Q18046320 property:P688 ?h }
Androglobin
Androglobin is encoded by ADGB
Androglobin
action filter_type
action find
entity ADGB
relation encodes
type nutrient
['ADGB', 'encodes', {'concept': 'nutrient'}]
SELECT DISTINCT ?h WHERE { ?h rdf:type ontology:nutrient . resource:ADGB property:encodes ?h }
[]
Simple Question (Coreferenced)
Simple Question|Single Entity|Indirect
Q21131625
P681
Q5058355
USER
What is a component of that nutrient ?
(Q21131625,P681,c(Q5058355))
action filter_type
action find
entity Q21131625
relation P681
type Q5058355
['Q21131625', 'P681', {'concept': 'Q5058355'}]
SELECT DISTINCT ?z WHERE { resource:Q21131625 property:P681 ?z . ?z rdf:type ontology:Q5058355 }
Androglobin
action filter_type
action find
entity Androglobin
relation cell component
type cellular component
['Androglobin', 'cell component', {'concept': 'cellular component'}]
SELECT DISTINCT ?z WHERE { resource:Androglobin property:cell_component ?z . ?z rdf:type ontology:cellular_component }
[]
cellular component
Q3824358
SYSTEM
intracellular
Q3824358
(Q21131625,P681,c(Q5058355))
action filter_type
action find
entity Q21131625
relation P681
type Q5058355
A component of that nutrient is an [ANSWER]
['Q21131625', 'P681', {'concept': 'Q5058355'}]
SELECT DISTINCT ?z WHERE { resource:Q21131625 property:P681 ?z . ?z rdf:type ontology:Q5058355 }
intracellular
A component of that nutrient is an intracellular
intracellular
action filter_type
action find
entity Androglobin
relation cell component
type cellular component
['Androglobin', 'cell component', {'concept': 'cellular component'}]
SELECT DISTINCT ?z WHERE { resource:Androglobin property:cell_component ?z . ?z rdf:type ontology:cellular_component }
[]
Simple Question (Ellipsis)
only subject is changed, parent and predicate remains same
Q21497400
Q5058355
USER
And what about Cytochrome P450 4B1?
(Q21497400,P681,c(Q5058355))
action filter_type
action find
entity Q21497400
relation P681
type Q5058355
['Q21497400', 'P681', {'concept': 'Q5058355'}]
SELECT DISTINCT ?b WHERE { resource:Q21497400 property:P681 ?b . ?b rdf:type ontology:Q5058355 }
Cytochrome P450 4B1
action filter_type
action find
entity Cytochrome P450 4B1
relation cell component
type cellular component
['Cytochrome P450 4B1', 'cell component', {'concept': 'cellular component'}]
SELECT DISTINCT ?b WHERE { resource:Cytochrome_P450_4B1 property:cell_component ?b . ?b rdf:type ontology:cellular_component }
[]
cellular component
Q79927 Q14329032 Q14878067
SYSTEM
endoplasmic reticulum, endoplasmic reticulum membrane, organelle membrane
Q79927 Q14329032 Q14878067
(Q21497400,P681,c(Q5058355))
action filter_type
action find
entity Q21497400
relation P681
type Q5058355
[ANSWERS]
['Q21497400', 'P681', {'concept': 'Q5058355'}]
SELECT DISTINCT ?b WHERE { resource:Q21497400 property:P681 ?b . ?b rdf:type ontology:Q5058355 }
endoplasmic reticulum endoplasmic reticulum membrane organelle membrane
endoplasmic reticulum endoplasmic reticulum membrane organelle membrane
action filter_type
action find
entity Cytochrome P450 4B1
relation cell component
type cellular component
['Cytochrome P450 4B1', 'cell component', {'concept': 'cellular component'}]
SELECT DISTINCT ?b WHERE { resource:Cytochrome_P450_4B1 property:cell_component ?b . ?b rdf:type ontology:cellular_component }
[]
Simple Question (Coreferenced)
Simple Question|Mult. Entity
Q79927 Q14329032 Q14878067
P361
Q5058355
USER
Which cellular components are those ones a component of ?
(Q79927,P361,c(Q5058355)) (Q14329032,P361,c(Q5058355)) (Q14878067,P361,c(Q5058355))
action filter_type
action find
entity prev_answer
relation P361
type Q5058355
['Q79927', 'P361', {'concept': 'Q5058355'}] ['Q14329032', 'P361', {'concept': 'Q5058355'}] ['Q14878067', 'P361', {'concept': 'Q5058355'}]
SELECT DISTINCT ?h WHERE { VALUES ( ?p ) { ( resource:Q79927 ) ( resource:Q14329032 ) ( resource:Q14878067 ) } . ?h rdf:type ontology:Q5058355 . ?p property:P361 ?h }
endoplasmic reticulum endoplasmic reticulum membrane organelle membrane
action filter_type
action find
entity prev_answer
relation part of
type cellular component
['endoplasmic reticulum', 'part of', {'concept': 'cellular component'}] ['endoplasmic reticulum membrane', 'part of', {'concept': 'cellular component'}] ['organelle membrane', 'part of', {'concept': 'cellular component'}]
SELECT DISTINCT ?h WHERE { VALUES ( ?p ) { ( resource:endoplasmic_reticulum ) ( resource:endoplasmic_reticulum_membrane ) ( resource:organelle_membrane ) } . ?h rdf:type ontology:cellular_component . ?p property:part_of ?h }
[]
cellular component
Q899827 Q21109092 Q21423046
SYSTEM
endomembrane system, nuclear outer membrane-endoplasmic reticulum membrane network, membrane-bounded organelle
Q899827 Q21109092 Q21423046
(Q79927,P361,c(Q5058355)) (Q14329032,P361,c(Q5058355)) (Q14878067,P361,c(Q5058355))
action filter_type
action find
entity prev_answer
relation P361
type Q5058355
[ANSWERS] are those ones a component of
['Q79927', 'P361', {'concept': 'Q5058355'}] ['Q14329032', 'P361', {'concept': 'Q5058355'}] ['Q14878067', 'P361', {'concept': 'Q5058355'}]
SELECT DISTINCT ?h WHERE { VALUES ( ?p ) { ( resource:Q79927 ) ( resource:Q14329032 ) ( resource:Q14878067 ) } . ?h rdf:type ontology:Q5058355 . ?p property:P361 ?h }
endomembrane system nuclear outer membrane-endoplasmic reticulum membrane network membrane-bounded organelle
Endomembrane system, nuclear outer membrane-endoplasmic reticulum membrane network and membrane-bounded organelle are those ones a component of
endomembrane system nuclear outer membrane-endoplasmic reticulum membrane network membrane-bounded organelle
action filter_type
action find
entity prev_answer
relation part of
type cellular component
['endoplasmic reticulum', 'part of', {'concept': 'cellular component'}] ['endoplasmic reticulum membrane', 'part of', {'concept': 'cellular component'}] ['organelle membrane', 'part of', {'concept': 'cellular component'}]
SELECT DISTINCT ?h WHERE { VALUES ( ?p ) { ( resource:endoplasmic_reticulum ) ( resource:endoplasmic_reticulum_membrane ) ( resource:organelle_membrane ) } . ?h rdf:type ontology:cellular_component . ?p property:part_of ?h }
[]
Simple Question (Direct)
Simple Question|Single Entity
Q15978631
P689
Q2057971
USER
Which health problem afflicts Homo sapiens ?
(c(Q2057971),P689,Q15978631)
action filter_type
action find_reverse
entity Q15978631
relation P689
type Q2057971
[{'concept': 'Q2057971'}, 'P689', 'Q15978631']
SELECT DISTINCT ?f WHERE { ?f property:P689 resource:Q15978631 . ?f rdf:type ontology:Q2057971 }
Homo sapiens
action filter_type
action find_reverse
entity Homo sapiens
relation afflicts
type health problem
[{'concept': 'health problem'}, 'afflicts', 'Homo sapiens']
SELECT DISTINCT ?f WHERE { ?f property:afflicts resource:Homo_sapiens . ?f rdf:type ontology:health_problem }
[]
health problem
Q403463
SYSTEM
Aicardi syndrome
Q403463
(c(Q2057971),P689,Q15978631)
action filter_type
action find_reverse
entity Q15978631
relation P689
type Q2057971
[ANSWER] afflicts Homo sapiens
[{'concept': 'Q2057971'}, 'P689', 'Q15978631']
SELECT DISTINCT ?f WHERE { ?f property:P689 resource:Q15978631 . ?f rdf:type ontology:Q2057971 }
Aicardi syndrome
Aicardi syndrome afflicts Homo sapiens
Aicardi syndrome
action filter_type
action find_reverse
entity Homo sapiens
relation afflicts
type health problem
[{'concept': 'health problem'}, 'afflicts', 'Homo sapiens']
SELECT DISTINCT ?f WHERE { ?f property:afflicts resource:Homo_sapiens . ?f rdf:type ontology:health_problem }
[]
Simple Question (Coreferenced)
Simple Question|Single Entity|Indirect
Q403463
P1995
Q1047113
USER
Which special field is the medical expertise concerned with that health problem ?
(Q403463,P1995,c(Q1047113))
action filter_type
action find
entity Q403463
relation P1995
type Q1047113
['Q403463', 'P1995', {'concept': 'Q1047113'}]
SELECT DISTINCT ?k WHERE { resource:Q403463 property:P1995 ?k . ?k rdf:type ontology:Q1047113 }
Aicardi syndrome
action filter_type
action find
entity Aicardi syndrome
relation medical specialty
type special field
['Aicardi syndrome', 'medical specialty', {'concept': 'special field'}]
SELECT DISTINCT ?k WHERE { resource:Aicardi_syndrome property:medical_specialty ?k . ?k rdf:type ontology:special_field }
[]
special field
Q1071953
SYSTEM
medical genetics
Q1071953
(Q403463,P1995,c(Q1047113))
action filter_type
action find
entity Q403463
relation P1995
type Q1047113
[ANSWER] is the medical expertise concerned with that health problem
['Q403463', 'P1995', {'concept': 'Q1047113'}]
SELECT DISTINCT ?k WHERE { resource:Q403463 property:P1995 ?k . ?k rdf:type ontology:Q1047113 }
medical genetics
Medical genetics is the medical expertise concerned with that health problem
medical genetics
action filter_type
action find
entity Aicardi syndrome
relation medical specialty
type special field
['Aicardi syndrome', 'medical specialty', {'concept': 'special field'}]
SELECT DISTINCT ?k WHERE { resource:Aicardi_syndrome property:medical_specialty ?k . ?k rdf:type ontology:special_field }
[]
Quantitative Reasoning (Count) (All)
Quantitative|Count|Single entity type|Indirect
P1995
Q2057971
USER
How many health problems have that special field as the associated medical expertise ?
(c(Q2057971),P1995,Q1071953)
action count
action filter_type
action find_reverse
entity Q1071953
relation P1995
type Q2057971
[{'concept': 'Q2057971'}, 'P1995', 'Q1071953']
SELECT DISTINCT ( COUNT ( ?x ) AS ?a ) WHERE { ?x property:P1995 resource:Q1071953 . ?x rdf:type ontology:Q2057971 }
action count
action filter_type
action find_reverse
entity medical genetics
relation medical specialty
type health problem
[{'concept': 'health problem'}, 'medical specialty', 'medical genetics']
SELECT DISTINCT ( COUNT ( ?x ) AS ?a ) WHERE { ?x property:medical_specialty resource:medical_genetics . ?x rdf:type ontology:health_problem }
[]
health problem
SYSTEM
261
Q2035109 Q5182137 Q3726816 Q3765145 Q557552 Q1477777 Q525075 Q2155008 Q17002116 Q208562 Q1332448 Q1538227 Q431643 Q2019823 Q6422092 Q3726862 Q1136492 Q2532540 Q1331116 Q6744609 Q17091221 Q6934642 Q484631 Q1543446 Q635339 Q1132108 Q2027937 Q1741965 Q1097490 Q1469646 Q4673593 Q525642 Q3709312 Q119280 Q749409 Q5959327 Q281115 Q884590 Q459896 Q653200 Q3251367 Q492129 Q390211 Q222634 Q2163245 Q779250 Q1133289 Q3026420 Q1786496 Q838139 Q584265 Q3886247 Q1343645 Q1459821 Q17001349 Q1495674 Q7578960 Q378183 Q2989168 Q17120550 Q669435 Q478891 Q752298 Q2388598 Q298233 Q388628 Q7320761 Q1678281 Q5147822 Q9390284 Q17009830 Q580506 Q340594 Q1641486 Q733493 Q1640324 Q1363508 Q2280106 Q940210 Q579527 Q303123 Q202849 Q594013 Q1141499 Q1456383 Q622427 Q1052391 Q914389 Q498487 Q1023604 Q221472 Q574741 Q209049 Q2033532 Q1787020 Q863861 Q1031536 Q5463847 Q1356194 Q4943512 Q1915681 Q3731836 Q1958739 Q1770836 Q521863 Q1077955 Q4731121 Q4821698 Q207133 Q998273 Q1952467 Q633859 Q1269307 Q17125860 Q5134736 Q1877483 Q18211695 Q3804555 Q923020 Q1587881 Q2735907 Q1452604 Q973524 Q844717 Q3567797 Q7234988 Q13566985 Q1640632 Q1970052 Q548719 Q1027995 Q47715 Q769988 Q741315 Q1130519 Q896643 Q619428 Q3395618 Q6705425 Q2272470 Q3047124 Q1476789 Q1283054 Q3043817 Q1162164 Q1410864 Q4597494 Q2200977 Q1409611 Q277452 Q1126831 Q744790 Q17010866 Q361648 Q585011 Q1418152 Q17010855 Q16934669 Q3801491 Q2288646 Q4305015 Q847605 Q662298 Q3589131 Q666980 Q1996246 Q2732398 Q246002 Q6673122 Q1583485 Q1101694 Q457737 Q1557239 Q1153641 Q3725646 Q781618 Q189167 Q616087 Q1536720 Q403463 Q7688951 Q1544989 Q548213 Q1112977 Q3124960 Q246040 Q1076060 Q579665 Q2072063 Q385774 Q1755537 Q939364 Q322370 Q8061303 Q2557206 Q4118166 Q535364 Q966052 Q883850 Q2273662 Q1360044 Q757749 Q2291208 Q5334295 Q1544416 Q1755568 Q4348144 Q1544408 Q2565270 Q1774751 Q1362721 Q5172184 Q3071315 Q3357668 Q618246 Q386346 Q7900616 Q3360152 Q1151801 Q1641399 Q612693 Q5375429 Q16550087 Q4420146 Q1475743 Q558077 Q572695 Q4646476 Q4675784 Q3508764 Q662185 Q610075 Q1462309 Q17163513 Q15443105 Q3335660 Q371520 Q659033 Q2823145 Q3508578 Q3961678 Q1327273 Q194101 Q1106881 Q182005 Q5465742 Q667681 Q284219 Q2142496 Q1699007 Q916398 Q7170412 Q1233526 Q7578540 Q178194 Q268292 Q1140794 Q193003 Q3179593 Q1584110 Q1257011
(c(Q2057971),P1995,Q1071953)
action count
action filter_type
action find_reverse
entity Q1071953
relation P1995
type Q2057971
[ANSWER]
[{'concept': 'Q2057971'}, 'P1995', 'Q1071953']
SELECT DISTINCT ( COUNT ( ?x ) AS ?a ) WHERE { ?x property:P1995 resource:Q1071953 . ?x rdf:type ontology:Q2057971 }
nail-patella syndrome Craniofacial abnormality epiblepharon ichthyosis vulgaris ankyloglossia osteopoikilosis hamartoma Ritscher-Schinzel syndrome fetal alcohol spectrum disorder Marfan syndrome Ellis–van Creveld syndrome Kabuki syndrome microcephaly Potter sequence Kniest dysplasia junctional epidermolysis bullosa Costello syndrome Birt-Hogg-Dube syndrome Alport syndrome 3MC syndrome 3 Hypoplastic right heart syndrome Multicystic dysplastic kidney imperforate anus Noonan syndrome Conorhyland hypospadias choledochal cyst Kindler syndrome cardiofaciocutaneous syndrome Bloom syndrome acheiropody DiGeorge syndrome dyskeratosis congenita Medullary sponge kidney osteogenesis imperfecta hypochondrogenesis Proteus syndrome Incontinentia pigmenti cystic lymphangioma flat feet problems osteochondrodysplasia porencephaly atrioventricular septal defect orofacial cleft congenital diaphragmatic hernia Crouzon syndrome Cornelia de Lange syndrome Diastematomyelia Acrocephalosyndactylia ventricular septal defect congenital nervous system abnormality Urticaria pigmentosa Hirschsprung's disease holoprosencephaly Cervical agenesis gastroschisis Spondyloepiphyseal dysplasia congenita Craniosynostosis hair disease peeling skin syndrome renal agenesis Simpson-Golabi-Behmel syndrome Cri du chat Ollier disease esophageal atresia Meckel's diverticulum Rhizomelic chondrodysplasia punctata Bardet-Biedl syndrome Coloboma of optic nerve Netherton syndrome Progestin-induced virilisation keratosis follicularis achondroplasia Marie Unna hereditary hypotrichosis Dandy-Walker syndrome hydrophthalmos monilethrix Branchio-oto-renal syndrome Hay–Wells syndrome pulmonary valve stenosis Aarskog-Scott syndrome Turner syndrome Prader-Willi syndrome Ehlers–Danlos syndrome situs inversus ptosis pseudoxanthoma elasticum Cockayne syndrome Camurati-Engelmann disease CHARGE syndrome fragile X syndrome Dubowitz syndrome chromosome 1q21.1 deletion syndrome Van der Woude syndrome thanatophoric dysplasia Hailey-Hailey disease campomelic dysplasia focal dermal hypoplasia Ectopia cordis Boomerang dysplasia Meckel syndrome congenital ichthyosiform erythroderma persistent Mullerian duct syndrome Sotos syndrome Beckwith-Wiedemann syndrome Hypohidrotic ectodermal dysplasia Allan-Herndon-Dudley syndrome spondylocostal dysostosis Klinefelter's syndrome Smith–Lemli–Opitz syndrome hereditary multiple exostoses Poland syndrome dysostosis Patella bipartita Cloacal exstrophy Congenital pulmonary venous return anomaly vaginal hypoplasia X-linked ichthyosis epidermolysis bullosa popliteal pterygium syndrome Cutis laxa Multiple epiphyseal dysplasia spondylolisthesis spina bifida hereditary mucosal leukokeratosis chromosome 17q21.31 duplication syndrome metaphyseal dysplasia Labial fusion Shwachman-Diamond syndrome Aniridia Pyloric stenosis Down syndrome Goldenhar syndrome Von Hippel–Lindau disease heart valve disease brachydactyly SC phocomelia syndrome Autosomal recessive polycystic kidney Lutembacher's syndrome Carpenter syndrome Ectopic testis jaw-winking syndrome hypochondroplasia Scaphocephaly clubfoot fibrous dysplasia intestinal atresia Miller-Dieker lissencephaly syndrome Port-wine stain Ebstein's anomaly tetralogy of Fallot Treacher Collins syndrome achondrogenesis type II Double outlet right ventricle Antley-Bixler syndrome Mobius syndrome achondrogenesis type IB heart septal defect epidermolytic hyperkeratosis Stickler syndrome buphthalmos neurofibromatosis ectropion epidermolysis bullosa dystrophica Rubinstein-Taybi syndrome hereditary lymphedema Autosomal dominant polycystic kidney polycystic liver disease thyroid gland disease Rothmund-Thomson syndrome Joubert syndrome Edwards syndrome‎ microphthalmia Wolfram syndrome midface dysplasia cleidocranial dysplasia Zellweger syndrome aortic valve insufficiency Nevoid basal cell carcinoma syndrome Aicardi syndrome Taussig–Bing syndrome Peutz-Jeghers syndrome neural tube defect syringomyelia epidermolysis bullosa simplex congenital cystic adenomatoid malformation chondrodysplasia punctata dextrocardia patent ductus arteriosus Townes-Brocks syndrome VACTERL association congenital heart disease ablepharon Yunis-Varon syndrome scimitar syndrome Polyostotic fibrous dysplasia Angelman syndrome cryptorchidism blepharophimosis pseudohermaphroditism syndactyly atrial heart septal defect Sjögren–Larsson syndrome ectopic thymus lissencephaly osteopetrosis Weaver syndrome Alagille syndrome hydranencephaly Klippel-Feil syndrome tuberous sclerosis coronary artery anomaly fibrochondrogenesis agnathia-otocephaly complex Apert syndrome tethered spinal cord syndrome bladder disease pachyonychia congenita Waardenburg syndrome hypoplastic left heart syndrome xeroderma pigmentosum Enchondromatosis Langer mesomelic dysplasia short rib – polydactyly syndrome Robinow syndrome Williams Syndrome Eisenmenger's syndrome Kleefstra syndrome acrokeratosis verruciformis Hand-Foot-Genital Syndrome choanal atresia Wolf-Hirschhorn syndrome Coloboma Pachygyria Polycystic kidney disease 3-M syndrome polydactyly biliary atresia achondrogenesis rapadilino syndrome Laurence-Moon syndrome Entropion dwarfism Coffin-Lowry syndrome Holt-Oram syndrome foot deformity Neu-Laxova syndrome Patau syndrome Silver–Russell syndrome Johanson–Blizzard syndrome lymphedema persistent hyperplastic primary vitreous osteosclerosis splenic disease cystic fibrosis mitral valve insufficiency mitral valve stenosis hydrocephalus skin tag arteriovenous malformation Nephronophthisis
261
action count
action filter_type
action find_reverse
entity medical genetics
relation medical specialty
type health problem
[{'concept': 'health problem'}, 'medical specialty', 'medical genetics']
SELECT DISTINCT ( COUNT ( ?x ) AS ?a ) WHERE { ?x property:medical_specialty resource:medical_genetics . ?x rdf:type ontology:health_problem }
[]