What is {genetic association} of {regulates (molecular biology)} of {hsa-miR-335-3p} ?
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SELECT ?p WHERE { ?b property:genetic_association ?p . resource:hsa-miR-335-3p property:regulates_(molecular_biology) ?b }
SELECT ?answer WHERE { ?statement1 <http://www.w3.org/1999/02/22-rdf-syntax-ns#subject> <http://wikidata.dbpedia.org/resource/Q27594933> . ?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:Q27594933 wdt:P128 ?X . ?X wdt:P2293 ?answer}
obesity schizophrenia Meckel syndrome 13 orofaciodigital syndrome XVI obesity obesity smallpox amyotrophic lateral sclerosis Parkinson's disease obesity rheumatoid arthritis sexual dysfunction idiopathic pulmonary fibrosis dental caries primary ciliary dyskinesia 14 early infantile epileptic encephalopathy 57 obesity multiple endocrine neoplasia type 4 multiple sclerosis autosomal recessive limb-girdle muscular dystrophy autosomal recessive limb-girdle muscular dystrophy type 2F dilated cardiomyopathy 1L progeroid syndrome, Petty type spinocerebellar ataxia 47 asthma Nijmegen breakage syndrome-like disorder catecholaminergic polymorphic ventricular tachycardia 5 hereditary spastic paraplegia 61 systemic lupus erythematosus maturity-onset diabetes of the young type 14 colorectal cancer autosomal recessive nonsyndromic deafness 103 obesity autosomal dominant non-syndromic intellectual disability 18 Chronic obstructive pulmonary disease epilepsy migraine disorder coronary artery disease refractive error obesity obesity schizencephaly hereditary spastic paraplegia 13 Wagner's disease obesity obesity Pelger-Huet anomaly Hydrops-ectopic calcification-moth-eaten skeletal dysplasia acute myeloid leukemia thrombocytopenia 5 obesity attention deficit hyperactivity disorder intellectual disability-severe speech delay-mild dysmorphism syndrome smallpox esophageal cancer hereditary thrombocytopenia with normal platelets-hematological cancer predisposition syndrome multiple sclerosis spinocerebellar ataxia type 6 episodic ataxia type 2 Multiple familial trichoepithelioma Tricho–dento–osseous syndrome amelogenesis imperfecta type 4 human immunodeficiency virus infectious disease autosomal dominant non-syndromic intellectual disability 7 Fanconi anemia complementation group F prostate cancer LADD syndrome ulcerative colitis dystonia 25 asthma rheumatoid arthritis smallpox spinocerebellar ataxia type 19/22 Brugada syndrome 9 myotonic dystrophy coeliac disease chromosome 1p32-p31 deletion syndrome morbid obesity obesity arterial hypertension prostate cancer autosomal dominant non-syndromic intellectual disability 36 hereditary spastic paraplegia 4 primary biliary cirrhosis congenital bile acid synthesis defect 2 hypogonadotropic hypogonadism 11 with or without anosmia Forney robinson pascoe syndrome Frontometaphyseal dysplasia 2; FMD2 systemic lupus erythematosus psoriasis spondyloepimetaphyseal dysplasia, Pakistani type CEDNIK syndrome