@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:NP857963.RAAJ1wgIR0amaeEuL-JWRxR4ZU0KX5VoJDQdLP9zfRyQg130_head { this: np:hasAssertion dgn-np:NP857963.RAAJ1wgIR0amaeEuL-JWRxR4ZU0KX5VoJDQdLP9zfRyQg130_assertion; np:hasProvenance dgn-np:NP857963.RAAJ1wgIR0amaeEuL-JWRxR4ZU0KX5VoJDQdLP9zfRyQg130_provenance; np:hasPublicationInfo dgn-np:NP857963.RAAJ1wgIR0amaeEuL-JWRxR4ZU0KX5VoJDQdLP9zfRyQg130_publicationInfo; a np:Nanopublication . dgn-np:NP857963.RAAJ1wgIR0amaeEuL-JWRxR4ZU0KX5VoJDQdLP9zfRyQg130_assertion a np:Assertion . dgn-np:NP857963.RAAJ1wgIR0amaeEuL-JWRxR4ZU0KX5VoJDQdLP9zfRyQg130_provenance a np:Provenance . dgn-np:NP857963.RAAJ1wgIR0amaeEuL-JWRxR4ZU0KX5VoJDQdLP9zfRyQg130_publicationInfo a np:PublicationInfo . } dgn-np:NP857963.RAAJ1wgIR0amaeEuL-JWRxR4ZU0KX5VoJDQdLP9zfRyQg130_assertion { miriam-gene:3553 a ncit:C16612 . lld:C0029410 a ncit:C7057 . dgn-gda:DGN5bee0edb0670bec720a3e5bfd44d36eb sio:SIO_000628 miriam-gene:3553, lld:C0029410; a sio:SIO_001122 . } dgn-np:NP857963.RAAJ1wgIR0amaeEuL-JWRxR4ZU0KX5VoJDQdLP9zfRyQg130_provenance { dgn-np:NP857963.RAAJ1wgIR0amaeEuL-JWRxR4ZU0KX5VoJDQdLP9zfRyQg130_assertion dcterms:description "[The meta-analysis of six published studies retrieved from the literature search and eight unpublished studies showed no evidence of association between common genetic variation in the IL1B or IL1RN genes and risk of hip OA or knee OA (P>0.05 for rs16944, rs1143634, rs419598 and haplotype C-G-C (rs1143634, rs16944 and rs419598) previously implicated in risk of hip OA).]. 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:21146623; 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:NP857963.RAAJ1wgIR0amaeEuL-JWRxR4ZU0KX5VoJDQdLP9zfRyQg130_publicationInfo { this: dcterms:created "2016-05-13T12:48:13+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" . }