@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:DGNb9a922a1d2d3cbfd16533906479485a3 sio:SIO_000628 miriam-gene:6584, lld:C0009324; a sio:SIO_001122 . } sub:provenance { sub:assertion dcterms:description "[A statistically significant increase in the risk of UC was detected in a recessive model of inheritances for OCTN1 (OR�=�1.23, 95% CI�=�1.08-1.40, P�<�0.001), OCTN2 (OR�=�1.18, 95% CI�=�1.05-1.33, P�=�0.006), IGR2096a_1 (OR�=�1.37, 95% CI�=�1.15-1.62, P�<�0.001) and IGR2198a_1 (OR�=�1.35, 95% CI�=�1.10-1.66, P�=�0.004); the increased risks of UC were maintained in the adult and Caucasian subgroups, but not the pediatric subgroup.]. 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" . }