@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:DGN6c9e7b466c4fcab228017b8ddac199b2 sio:SIO_000628 miriam-gene:6584, lld:C0010346; a sio:SIO_001122 . } sub:provenance { sub:assertion dcterms:description "[Overall, five IBD5 variants in a per-allele model of inheritance were significantly associated with elevated CD risk (for OCTN1: OR�=�1.23, 95% CI�=�1.16-1.30, P�<�0.001; for OCTN2: OR�=�1.20, 95% CI�=�1.11-1.30, P�<�0.001; for IGR2096a_1: OR�=�1.36, 95% CI�=�1.24-1.46, P�<�0.001; for IGR2198a_1: OR�=�1.34, 95% CI�=�1.24-1.46, P�<�0.001; for IGR2230a_1: OR�=�1.35, 95% CI�=�1.23-1.48, P�<�0.001) and OCTN1/2 TC haplotype (OR�=�1.32, 95% CI�=�1.22-1.43, P�<�0.001).]. 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:21279723; 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 "2017-10-17T13:16:18+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" . }