Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP577277.RAP1VMSUJsVVeSdqjAyM7l23DCJGpQKwcDTA3PRCxmJAA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP577277.RAP1VMSUJsVVeSdqjAyM7l23DCJGpQKwcDTA3PRCxmJAA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP577277.RAP1VMSUJsVVeSdqjAyM7l23DCJGpQKwcDTA3PRCxmJAA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP577277.RAP1VMSUJsVVeSdqjAyM7l23DCJGpQKwcDTA3PRCxmJAA130_provenance.
- NP577277.RAP1VMSUJsVVeSdqjAyM7l23DCJGpQKwcDTA3PRCxmJAA130_assertion description "[However, the combined variant genotypes of the four loci with P(trend) approaching to 0.10 (rs2228526, rs4253160, rs12571445 and rs3793784) were associated with a significantly increased lung cancer risk (adjusted OR 1.35, 95% CI, 1.04-1.75 among subjects carrying three or more variant alleles), indicating that multiple loci in ERCC6 may jointly contribute to the susceptibility of lung cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP577277.RAP1VMSUJsVVeSdqjAyM7l23DCJGpQKwcDTA3PRCxmJAA130_provenance.
- NP577277.RAP1VMSUJsVVeSdqjAyM7l23DCJGpQKwcDTA3PRCxmJAA130_assertion evidence source_evidence_literature NP577277.RAP1VMSUJsVVeSdqjAyM7l23DCJGpQKwcDTA3PRCxmJAA130_provenance.
- NP577277.RAP1VMSUJsVVeSdqjAyM7l23DCJGpQKwcDTA3PRCxmJAA130_assertion SIO_000772 18789574 NP577277.RAP1VMSUJsVVeSdqjAyM7l23DCJGpQKwcDTA3PRCxmJAA130_provenance.
- NP577277.RAP1VMSUJsVVeSdqjAyM7l23DCJGpQKwcDTA3PRCxmJAA130_assertion wasDerivedFrom befree-20140225 NP577277.RAP1VMSUJsVVeSdqjAyM7l23DCJGpQKwcDTA3PRCxmJAA130_provenance.
- NP577277.RAP1VMSUJsVVeSdqjAyM7l23DCJGpQKwcDTA3PRCxmJAA130_assertion wasGeneratedBy ECO_0000203 NP577277.RAP1VMSUJsVVeSdqjAyM7l23DCJGpQKwcDTA3PRCxmJAA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP577277.RAP1VMSUJsVVeSdqjAyM7l23DCJGpQKwcDTA3PRCxmJAA130_provenance.