Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP803279.RA1bZDt54h0ez0DRQz66TAc5E94x6hA3dFbQGlWZHrPPM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP803279.RA1bZDt54h0ez0DRQz66TAc5E94x6hA3dFbQGlWZHrPPM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP803279.RA1bZDt54h0ez0DRQz66TAc5E94x6hA3dFbQGlWZHrPPM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP803279.RA1bZDt54h0ez0DRQz66TAc5E94x6hA3dFbQGlWZHrPPM130_provenance.
- NP803279.RA1bZDt54h0ez0DRQz66TAc5E94x6hA3dFbQGlWZHrPPM130_assertion description "[Family history of ovarian cancer was a strong predictor of a BRCA1/2 mutation (OR = 8.3; p = 0.01), however, family history of breast cancer was not indicative of carrier status.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP803279.RA1bZDt54h0ez0DRQz66TAc5E94x6hA3dFbQGlWZHrPPM130_provenance.
- NP803279.RA1bZDt54h0ez0DRQz66TAc5E94x6hA3dFbQGlWZHrPPM130_assertion evidence source_evidence_literature NP803279.RA1bZDt54h0ez0DRQz66TAc5E94x6hA3dFbQGlWZHrPPM130_provenance.
- NP803279.RA1bZDt54h0ez0DRQz66TAc5E94x6hA3dFbQGlWZHrPPM130_assertion SIO_000772 20353281 NP803279.RA1bZDt54h0ez0DRQz66TAc5E94x6hA3dFbQGlWZHrPPM130_provenance.
- NP803279.RA1bZDt54h0ez0DRQz66TAc5E94x6hA3dFbQGlWZHrPPM130_assertion wasDerivedFrom befree-2016 NP803279.RA1bZDt54h0ez0DRQz66TAc5E94x6hA3dFbQGlWZHrPPM130_provenance.
- NP803279.RA1bZDt54h0ez0DRQz66TAc5E94x6hA3dFbQGlWZHrPPM130_assertion wasGeneratedBy ECO_0000203 NP803279.RA1bZDt54h0ez0DRQz66TAc5E94x6hA3dFbQGlWZHrPPM130_provenance.
- befree-2016 importedOn "2016-02-19" NP803279.RA1bZDt54h0ez0DRQz66TAc5E94x6hA3dFbQGlWZHrPPM130_provenance.