sub:provenance {
sub:assertion dcterms:description "[The risk of anemia was increased for variant alleles of rs1128503 (ABCB1, C?>?T; p?=?0.023, OR?=?1.71, 95% CI?=?1.07-2.71), rs363717 (ABCA1, A?>?G; p?=?0.002, OR?=?2.08, 95% CI?=?1.32-3.27) and rs11615 (ERCC1, T?>?C; p?=?0.031, OR?=?1.61, 95% CI?=?1.04-2.50), while it was decreased for variant alleles of rs12762549 (ABCC2, C?>?G; p?=?0.004, OR?=?0.51, 95% CI?=?0.33-0.81).]. 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:25881102 ;
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 .
}