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 .
}