What is {genetic association} of {regulates (molecular biology)} of {hsa-miR-5006-3p} ?
Where does hsa-miR-5006-3p come from in molecular biology?
Who regulates the genetic association of hsa-miR-5006-3p in molecular biology
SELECT ?e WHERE { resource:hsa-miR-5006-3p property:regulates_(molecular_biology) ?q . ?q property:genetic_association ?e }
SELECT ?answer WHERE { ?statement1 <http://www.w3.org/1999/02/22-rdf-syntax-ns#subject> <http://wikidata.dbpedia.org/resource/Q27593301> . ?statement1 <http://www.w3.org/1999/02/22-rdf-syntax-ns#predicate> <http://www.wikidata.org/entity/P128>. ?statement1 <http://www.w3.org/1999/02/22-rdf-syntax-ns#object> ?X . ?statement2 <http://www.w3.org/1999/02/22-rdf-syntax-ns#subject> ?X. ?statement2 <http://www.w3.org/1999/02/22-rdf-syntax-ns#predicate> <http://www.wikidata.org/entity/P2293> . ?statement2 <http://www.w3.org/1999/02/22-rdf-syntax-ns#object> ?answer . }
SELECT ?answer WHERE { wd:Q27593301 wdt:P128 ?X . ?X wdt:P2293 ?answer}
hereditary spastic paraplegia 53 breast cancer prostate cancer amyotrophic lateral sclerosis Parkinson's disease human immunodeficiency virus infectious disease rheumatoid arthritis autosomal recessive limb-girdle muscular dystrophy type 2Y cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome craniosynostosis cannabis dependence smallpox type 2 diabetes obesity coronary artery disease microphthalmia with limb anomalies obesity focal epilepsy anorexia nervosa bipolar disorder Kawasaki disease amyotrophic lateral sclerosis smallpox amyotrophic lateral sclerosis nemaline myopathy 8 Axenfeld-Rieger syndrome type 3 Koolen de Vries syndrome juvenile polyposis syndrome amyotrophic lateral sclerosis spinocerebellar ataxia type 1 schizophrenia major depressive disorders bipolar disorder Timothy syndrome Brugada syndrome 3 unipolar depression breast cancer bipolar disorder colorectal cancer coronary artery disease metabolic disease type 2 diabetes Aarskog syndrome smallpox esophageal cancer hereditary thrombocytopenia with normal platelets-hematological cancer predisposition syndrome allergy reticular dysgenesis stroke Kawasaki disease coronary artery disease cerebrovascular disease obesity epilepsy prune belly syndrome Miller syndrome spinocerebellar ataxia type 26 coeliac disease chromosome 1p32-p31 deletion syndrome refractive error branchiootorenal syndrome autosomal dominant nonsyndromic deafness 23 coronary artery disease X-linked intellectual disability Alzheimer's disease spinocerebellar ataxia type 42 amyotrophic lateral sclerosis morbid obesity Crohn's disease leprosy inflammatory bowel diseases primary biliary cirrhosis type-1 diabetes rheumatoid arthritis coronary artery disease human immunodeficiency virus infectious disease alcohol abuse Floating-Harbor syndrome smallpox periodontitis