Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP552451.RAUqnmp1Qa_U4EHBYDqRV0P5LskyHrvbO5KBsxOfO5c0g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP552451.RAUqnmp1Qa_U4EHBYDqRV0P5LskyHrvbO5KBsxOfO5c0g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP552451.RAUqnmp1Qa_U4EHBYDqRV0P5LskyHrvbO5KBsxOfO5c0g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP552451.RAUqnmp1Qa_U4EHBYDqRV0P5LskyHrvbO5KBsxOfO5c0g130_provenance.
- NP552451.RAUqnmp1Qa_U4EHBYDqRV0P5LskyHrvbO5KBsxOfO5c0g130_assertion description "[The variant allele for T241M (C>T) polymorphism in the XRCC3 gene was associated with a decreased cancer risk [odds ratio (OR), 0.73; 95% confidence interval (CI), 0.61-0.88; P = 0.0007, multiple testing corrected P = 0.004].]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP552451.RAUqnmp1Qa_U4EHBYDqRV0P5LskyHrvbO5KBsxOfO5c0g130_provenance.
- NP552451.RAUqnmp1Qa_U4EHBYDqRV0P5LskyHrvbO5KBsxOfO5c0g130_assertion evidence source_evidence_literature NP552451.RAUqnmp1Qa_U4EHBYDqRV0P5LskyHrvbO5KBsxOfO5c0g130_provenance.
- NP552451.RAUqnmp1Qa_U4EHBYDqRV0P5LskyHrvbO5KBsxOfO5c0g130_assertion SIO_000772 16501254 NP552451.RAUqnmp1Qa_U4EHBYDqRV0P5LskyHrvbO5KBsxOfO5c0g130_provenance.
- NP552451.RAUqnmp1Qa_U4EHBYDqRV0P5LskyHrvbO5KBsxOfO5c0g130_assertion wasDerivedFrom befree-20140225 NP552451.RAUqnmp1Qa_U4EHBYDqRV0P5LskyHrvbO5KBsxOfO5c0g130_provenance.
- NP552451.RAUqnmp1Qa_U4EHBYDqRV0P5LskyHrvbO5KBsxOfO5c0g130_assertion wasGeneratedBy ECO_0000203 NP552451.RAUqnmp1Qa_U4EHBYDqRV0P5LskyHrvbO5KBsxOfO5c0g130_provenance.
- befree-20140225 importedOn "2014-02-25" NP552451.RAUqnmp1Qa_U4EHBYDqRV0P5LskyHrvbO5KBsxOfO5c0g130_provenance.