@prefix this: . @prefix rdfs: . @prefix xsd: . @prefix sio: . @prefix ncit: . @prefix lld: . @prefix miriam-gene: . @prefix miriam-pubmed: . @prefix eco: . @prefix wi: . @prefix prov: . @prefix pav: . @prefix prv: . @prefix dcterms: . @prefix np: . @prefix dgn-np: . @prefix dgn-gda: . @prefix dgn-void: . dgn-np:NP1255329.RAtA4dbE1wtVJzPU6hY9T6eGN7ME5Zw0qWP0Ffu8dWQu4130_head { this: np:hasAssertion dgn-np:NP1255329.RAtA4dbE1wtVJzPU6hY9T6eGN7ME5Zw0qWP0Ffu8dWQu4130_assertion; np:hasProvenance dgn-np:NP1255329.RAtA4dbE1wtVJzPU6hY9T6eGN7ME5Zw0qWP0Ffu8dWQu4130_provenance; np:hasPublicationInfo dgn-np:NP1255329.RAtA4dbE1wtVJzPU6hY9T6eGN7ME5Zw0qWP0Ffu8dWQu4130_publicationInfo; a np:Nanopublication . dgn-np:NP1255329.RAtA4dbE1wtVJzPU6hY9T6eGN7ME5Zw0qWP0Ffu8dWQu4130_assertion a np:Assertion . dgn-np:NP1255329.RAtA4dbE1wtVJzPU6hY9T6eGN7ME5Zw0qWP0Ffu8dWQu4130_provenance a np:Provenance . dgn-np:NP1255329.RAtA4dbE1wtVJzPU6hY9T6eGN7ME5Zw0qWP0Ffu8dWQu4130_publicationInfo a np:PublicationInfo . } dgn-np:NP1255329.RAtA4dbE1wtVJzPU6hY9T6eGN7ME5Zw0qWP0Ffu8dWQu4130_assertion { miriam-gene:57706 a ncit:C16612 . lld:C0206081 a ncit:C7057 . dgn-gda:DGN6c973a6b26c6c617cbc68338ad35295b sio:SIO_000628 miriam-gene:57706, lld:C0206081; a sio:SIO_001122 . } dgn-np:NP1255329.RAtA4dbE1wtVJzPU6hY9T6eGN7ME5Zw0qWP0Ffu8dWQu4130_provenance { dgn-np:NP1255329.RAtA4dbE1wtVJzPU6hY9T6eGN7ME5Zw0qWP0Ffu8dWQu4130_assertion dcterms:description "[After adjustment for age and BMI, variants in luteinizing hormone/choriogonadotropin receptor (LHCGR) (rs13405728), C9orf3 (rs4385527) and insulin receptor gene (INSR) (rs2059807) were strongly associated with OA (Padjust < 0.01, <0.001 and <0.05, respectively); rs4385527 in C9orf3 was strongly associated with HA (Padjust< 0.001); variants in the thyroid adenoma associated gene (THADA) (rs13429458 and rs12478601), DENN/MADD domain containing 1A (DENND1A)(rs10818854), and C9orf3 (rs4385527) were significantly associated with PCOM (Padjust < 0.01, <0.001, <0.05 and <0.001, respectively).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en; wi:evidence dgn-void:source_evidence_literature; sio:SIO_000772 miriam-pubmed:25586784; prov:wasDerivedFrom dgn-void:befree-2016; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-2016 pav:importedOn "2016-02-19"^^xsd:date . dgn-void:source_evidence_literature a eco:ECO_0000212; rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en; rdfs:label "DisGeNET evidence - LITERATURE"@en . } dgn-np:NP1255329.RAtA4dbE1wtVJzPU6hY9T6eGN7ME5Zw0qWP0Ffu8dWQu4130_publicationInfo { this: dcterms:created "2016-05-13T12:51:15+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetv3.0rdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v4.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v4.0.0" . }