What is {genetic association} of {regulates (molecular biology)} of {hsa-miR-7110-3p} ?
Which is the hereditary affiliation that directs the atomic science of HSA-MIR-7110-3p?
Which is the genetic association that regulates the molecular biology of HSA-MIR-7110-3p?
SELECT ?g WHERE { resource:hsa-miR-7110-3p property:regulates_(molecular_biology) ?t . ?t property:genetic_association ?g }
SELECT ?answer WHERE { ?statement1 <http://www.w3.org/1999/02/22-rdf-syntax-ns#subject> <http://wikidata.dbpedia.org/resource/Q27594530> . ?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:Q27594530 wdt:P128 ?X . ?X wdt:P2293 ?answer}
obesity dilated cardiomyopathy 1DD methylmalonic acidemia cblB type methylmalonic acidemia without homocystinuria obesity refractive error rheumatoid arthritis Langer mesomelic dysplasia SHOX-related short stature schizophrenia obesity Hyper-IgM syndrome type 2 chronic lymphocytic leukemia psoriasis obesity autosomal dominant non-syndromic intellectual disability 41 Pierpont syndrome obesity obesity cone-rod dystrophy 5 obesity obesity smallpox amyotrophic lateral sclerosis juvenile absence epilepsy HIV/AIDS autism osteoarthritis ankylosing spondylitis Ellis–Van Creveld syndrome acrofacial dysostosis, Weyers type prostate cancer major depressive disorders Hennekam syndrome unipolar depression Bartter disease type 4a Noonan syndrome 2 Noonan syndrome 10 coronary artery disease bipolar disorder Joubert syndrome 25 hypothyroidism obesity obesity autosomal recessive osteopetrosis 5 syndromic X-linked intellectual disability Raymond type Pascual-Castroviejo syndrome rheumatoid arthritis type 2 diabetes alcohol dependence Alpha-aminoadipic and alpha-ketoadipic aciduria Charcot-Marie-Tooth disease axonal type 2Q hyperprolactinemia long chain acyl-CoA dehydrogenase deficiency arterial hypertension coronary artery disease periodontitis dilated cardiomyopathy 1AA Koolen de Vries syndrome acute myeloid leukemia myelodysplastic syndrome juvenile myelomonocytic leukemia Schinzel–Giedion syndrome autosomal dominant non-syndromic intellectual disability 29 antithrombin III deficiency type 1 diabetes mellitus 22 growth delay due to insulin-like growth factor I resistance multiple sclerosis psoriasis tuberous sclerosis lymphangioleiomyomatosis tuberous sclerosis 1 dental caries retinitis pigmentosa 41 cone-rod dystrophy 12 type 2 diabetes coronary artery disease Crohn's disease multiple sclerosis Hereditary cystatin C amyloid angiopathy age related macular degeneration 11 multiple sclerosis Müllerian agenesis breast cancer colorectal cancer Proteus syndrome Cowden syndrome 1 dystonia 12 multiple sclerosis non-small-cell lung carcinoma non-small-cell lung carcinoma smallpox Multiple familial trichoepithelioma deafness dystonia syndrome microcephaly progressive microcephaly-seizures-cortical blindness-developmental delay syndrome attention deficit hyperactivity disorder schizencephaly Bamforth-Lazarus syndrome early infantile epileptic encephalopathy 19 epilepsy Charcot–Marie–Tooth disease anorexia nervosa pancreatic cancer smallpox autosomal dominant non-syndromic intellectual disability 6 alcohol abuse smallpox spinocerebellar ataxia type 13 Keppen–Lubinsky syndrome alcohol abuse coeliac disease obesity smallpox vitiligo melanoma rheumatoid arthritis male infertility hypertension and brachydactyly syndrome prostate cancer Crohn's disease alcohol abuse obesity schizophrenia bipolar disorder myopia nonsyndromic deafness autosomal recessive nonsyndromic deafness 24 rheumatoid arthritis psoriatic arthritis multiple sclerosis age related macular degeneration cytochrome-c oxidase deficiency disease branchiootorenal syndrome autosomal dominant nonsyndromic deafness 23 Coffin-Siris syndrome 5