What is {genetic association} of {regulates (molecular biology)} of {hsa-miR-4446-5p} ?
who hereditary affiliation of directs atomic science of hsa-miR-4446-5p ?
who genetic association of regulates molecular biology of hsa-miR-4446-5p ?
SELECT ?y WHERE { resource:hsa-miR-4446-5p property:regulates_(molecular_biology) ?b . ?b property:genetic_association ?y }
SELECT ?answer WHERE { ?statement1 <http://www.w3.org/1999/02/22-rdf-syntax-ns#subject> <http://wikidata.dbpedia.org/resource/Q27594521> . ?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:Q27594521 wdt:P128 ?X . ?X wdt:P2293 ?answer}
Parkinson's disease human immunodeficiency virus infectious disease autosomal recessive limb-girdle muscular dystrophy type 2Y asthma early infantile epileptic encephalopathy 55 cannabis dependence smallpox type 2 diabetes Chronic obstructive pulmonary disease coronary artery disease microphthalmia with limb anomalies obesity anorexia nervosa bipolar disorder Kawasaki disease lymphoblastic leukemia amyotrophic lateral sclerosis hereditary spastic paraplegia 53 breast cancer schizophrenia bipolar disorder mental depression periodontitis dilated cardiomyopathy 1AA Axenfeld-Rieger syndrome type 3 gout gout attack antithrombin III deficiency Duchenne muscular dystrophy dilated cardiomyopathy 3B progressive muscular dystrophy amyotrophic lateral sclerosis spinocerebellar ataxia type 1 Chronic obstructive pulmonary disease Aarskog syndrome smallpox esophageal cancer hereditary thrombocytopenia with normal platelets-hematological cancer predisposition syndrome allergy mitochondrial complex V (ATP synthase) deficiency nuclear type 3 ulcerative colitis obesity fatty liver disease epilepsy prune belly syndrome spinocerebellar ataxia type 26 MEHMO syndrome obesity type-1 diabetes obesity factor v and Factor VIII, combined deficiency of, type 1 coeliac disease chromosome 1p32-p31 deletion syndrome rheumatoid arthritis psoriatic arthritis refractive error branchiootorenal syndrome autosomal dominant nonsyndromic deafness 23 schizencephaly holoprosencephaly 2 coronary artery disease Alzheimer's disease spinocerebellar ataxia type 42 amyotrophic lateral sclerosis morbid obesity Crohn's disease leprosy inflammatory bowel diseases primary biliary cirrhosis syndromic X-linked intellectual disability Turner type human immunodeficiency virus infectious disease Chronic obstructive pulmonary disease interstitial lung disease primary ciliary dyskinesia 29 alcohol abuse Floating-Harbor syndrome smallpox cardiovascular disease