@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1351920.RAG1Epw2eIxOVP3jtCXaGGZG0ZIv-qxViWGLE6-79ag4o> . @prefix sub: <http://rdf.disgenet.org/resource/nanopub/NP1351920.RAG1Epw2eIxOVP3jtCXaGGZG0ZIv-qxViWGLE6-79ag4o#> . @prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> . @prefix xsd: <http://www.w3.org/2001/XMLSchema#> . @prefix sio: <http://semanticscience.org/resource/> . @prefix lld: <http://linkedlifedata.com/resource/umls/id/> . @prefix miriam-gene: <http://identifiers.org/ncbigene/> . @prefix miriam-pubmed: <http://identifiers.org/pubmed/> . @prefix eco: <http://purl.obolibrary.org/obo/> . @prefix wi: <http://purl.org/ontology/wi/core#> . @prefix prov: <http://www.w3.org/ns/prov#> . @prefix pav: <http://purl.org/pav/> . @prefix prv: <http://purl.org/net/provenance/ns#> . @prefix dcterms: <http://purl.org/dc/terms/> . @prefix np: <http://www.nanopub.org/nschema#> . @prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> . @prefix dgn-void: <http://rdf.disgenet.org/v5.0.0/void/> . sub:head { this: np:hasAssertion sub:assertion; np:hasProvenance sub:provenance; np:hasPublicationInfo sub:publicationInfo; a np:Nanopublication . } sub:assertion { dgn-gda:DGN476c0347cc79880dc963c2fee28ed265 sio:SIO_000628 miriam-gene:57706, lld:C0003128; a sio:SIO_001122 . } sub:provenance { sub: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; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:BEFREE pav:importedOn "2017-02-19"^^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 . } sub:publicationInfo { this: dcterms:created "2017-10-17T13:18:46+02:00"^^xsd:dateTime; dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetv3.0rdf; pav:authoredBy <http://orcid.org/0000-0001-5999-6269>, <http://orcid.org/0000-0002-7534-7661>, <http://orcid.org/0000-0002-9383-528X>, <http://orcid.org/0000-0003-0169-8159>, <http://orcid.org/0000-0003-1244-7654>; pav:createdBy <http://orcid.org/0000-0003-0169-8159>; pav:version "v5.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v5.0.0" . }