Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP887927.RABJ097OGUqDyaIEaGXHJU8JOeA-sqTDn7lywoaT1f0hw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP887927.RABJ097OGUqDyaIEaGXHJU8JOeA-sqTDn7lywoaT1f0hw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP887927.RABJ097OGUqDyaIEaGXHJU8JOeA-sqTDn7lywoaT1f0hw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP887927.RABJ097OGUqDyaIEaGXHJU8JOeA-sqTDn7lywoaT1f0hw130_provenance.
- NP887927.RABJ097OGUqDyaIEaGXHJU8JOeA-sqTDn7lywoaT1f0hw130_assertion description "[The -2578C and -1154G alleles, which are both hypothesized to increase expression of VEGF, were associated with increased risk for invasive breast cancer (odds ratio [OR] 1.46, 95% confidence interval [CI] 1.00-2.14 for -2578 CC versus AA; OR 1.64, 95% CI 1.02-2.64 for -1154 GG versus AA) but they were not associated with risk for in situ cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP887927.RABJ097OGUqDyaIEaGXHJU8JOeA-sqTDn7lywoaT1f0hw130_provenance.
- NP887927.RABJ097OGUqDyaIEaGXHJU8JOeA-sqTDn7lywoaT1f0hw130_assertion evidence source_evidence_literature NP887927.RABJ097OGUqDyaIEaGXHJU8JOeA-sqTDn7lywoaT1f0hw130_provenance.
- NP887927.RABJ097OGUqDyaIEaGXHJU8JOeA-sqTDn7lywoaT1f0hw130_assertion SIO_000772 16613616 NP887927.RABJ097OGUqDyaIEaGXHJU8JOeA-sqTDn7lywoaT1f0hw130_provenance.
- NP887927.RABJ097OGUqDyaIEaGXHJU8JOeA-sqTDn7lywoaT1f0hw130_assertion wasDerivedFrom befree-20140225 NP887927.RABJ097OGUqDyaIEaGXHJU8JOeA-sqTDn7lywoaT1f0hw130_provenance.
- NP887927.RABJ097OGUqDyaIEaGXHJU8JOeA-sqTDn7lywoaT1f0hw130_assertion wasGeneratedBy ECO_0000203 NP887927.RABJ097OGUqDyaIEaGXHJU8JOeA-sqTDn7lywoaT1f0hw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP887927.RABJ097OGUqDyaIEaGXHJU8JOeA-sqTDn7lywoaT1f0hw130_provenance.