Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP499806.RA7jhhTcalt-S4GEijkGkEBK17B6F253xWyRsOXKlcMfM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP499806.RA7jhhTcalt-S4GEijkGkEBK17B6F253xWyRsOXKlcMfM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP499806.RA7jhhTcalt-S4GEijkGkEBK17B6F253xWyRsOXKlcMfM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP499806.RA7jhhTcalt-S4GEijkGkEBK17B6F253xWyRsOXKlcMfM130_provenance.
- NP499806.RA7jhhTcalt-S4GEijkGkEBK17B6F253xWyRsOXKlcMfM130_assertion description "[We found that the RAD52 2259 CT or TT, hMLH1 -93 GG, and ERCC1 8092 AA genotypes were associated with breast cancer risk after adjustment for known risk factors [odds ratio (OR), 1.33; 95% confidence interval (95% CI), 1.02-1.75; OR, 1.31; 95% CI, 0.99-1.74; and OR, 0.58; 95% CI, 0.38-0.89, respectively].]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP499806.RA7jhhTcalt-S4GEijkGkEBK17B6F253xWyRsOXKlcMfM130_provenance.
- NP499806.RA7jhhTcalt-S4GEijkGkEBK17B6F253xWyRsOXKlcMfM130_assertion evidence source_evidence_literature NP499806.RA7jhhTcalt-S4GEijkGkEBK17B6F253xWyRsOXKlcMfM130_provenance.
- NP499806.RA7jhhTcalt-S4GEijkGkEBK17B6F253xWyRsOXKlcMfM130_assertion SIO_000772 15958648 NP499806.RA7jhhTcalt-S4GEijkGkEBK17B6F253xWyRsOXKlcMfM130_provenance.
- NP499806.RA7jhhTcalt-S4GEijkGkEBK17B6F253xWyRsOXKlcMfM130_assertion wasDerivedFrom befree-2016 NP499806.RA7jhhTcalt-S4GEijkGkEBK17B6F253xWyRsOXKlcMfM130_provenance.
- NP499806.RA7jhhTcalt-S4GEijkGkEBK17B6F253xWyRsOXKlcMfM130_assertion wasGeneratedBy ECO_0000203 NP499806.RA7jhhTcalt-S4GEijkGkEBK17B6F253xWyRsOXKlcMfM130_provenance.
- befree-2016 importedOn "2016-02-19" NP499806.RA7jhhTcalt-S4GEijkGkEBK17B6F253xWyRsOXKlcMfM130_provenance.