@prefix this: . @prefix sub: . @prefix rdfs: . @prefix xsd: . @prefix sio: . @prefix lld: . @prefix miriam-gene: . @prefix miriam-pubmed: . @prefix eco: . @prefix wi: . @prefix prov: . @prefix pav: . @prefix prv: . @prefix dcterms: . @prefix np: . @prefix dgn-gda: . @prefix dgn-void: . sub:head { this: np:hasAssertion sub:assertion; np:hasProvenance sub:provenance; np:hasPublicationInfo sub:publicationInfo; a np:Nanopublication . } sub:assertion { dgn-gda:DGNd8872815e47597d043c319da51c6d4ec sio:SIO_000628 miriam-gene:3123, lld:C0018213; a sio:SIO_001122 . } sub:provenance { sub:assertion dcterms:description "[Combining the data of two sample populations, we found that B*46:01 (odds ratio under dominant model [OR] ?=?1.33, Bonferroni corrected combined P [P(Bc)] ?=?1.17 x 10?�), DPB1*05:01 (OR ?=?2.34, P(Bc)?=?2.58 x 10?�?), DQB1*03:02 (OR ?=?0.62, P(Bc) ?=?1.97 x 10?�), DRB1*15:01 (OR ?=?1.68, P(Bc)?=?1.22 x 10?�) and DRB1*16:02 (OR ?=?2.63, P(Bc) ?=?1.46 x 10??) were associated with GD.]. 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:21307958; 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 "2017-10-17T13:13:23+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 "v5.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v5.0.0" . }