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 .
}