Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP624199.RA2qfZ3CWEMGo9orqne8jFar05_p5fKz26EZnl7T0Fd8A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP624199.RA2qfZ3CWEMGo9orqne8jFar05_p5fKz26EZnl7T0Fd8A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP624199.RA2qfZ3CWEMGo9orqne8jFar05_p5fKz26EZnl7T0Fd8A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP624199.RA2qfZ3CWEMGo9orqne8jFar05_p5fKz26EZnl7T0Fd8A130_provenance.
- NP624199.RA2qfZ3CWEMGo9orqne8jFar05_p5fKz26EZnl7T0Fd8A130_assertion description "[For XPD, having variation at both loci (312Asn and 751Gln) occurred less frequently among BCC and SCC cases compared with controls (OR = 0.8; 95% CI, 0.6-1.0) for both case groups.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP624199.RA2qfZ3CWEMGo9orqne8jFar05_p5fKz26EZnl7T0Fd8A130_provenance.
- NP624199.RA2qfZ3CWEMGo9orqne8jFar05_p5fKz26EZnl7T0Fd8A130_assertion evidence source_evidence_literature NP624199.RA2qfZ3CWEMGo9orqne8jFar05_p5fKz26EZnl7T0Fd8A130_provenance.
- NP624199.RA2qfZ3CWEMGo9orqne8jFar05_p5fKz26EZnl7T0Fd8A130_assertion SIO_000772 17687452 NP624199.RA2qfZ3CWEMGo9orqne8jFar05_p5fKz26EZnl7T0Fd8A130_provenance.
- NP624199.RA2qfZ3CWEMGo9orqne8jFar05_p5fKz26EZnl7T0Fd8A130_assertion wasDerivedFrom befree-2016 NP624199.RA2qfZ3CWEMGo9orqne8jFar05_p5fKz26EZnl7T0Fd8A130_provenance.
- NP624199.RA2qfZ3CWEMGo9orqne8jFar05_p5fKz26EZnl7T0Fd8A130_assertion wasGeneratedBy ECO_0000203 NP624199.RA2qfZ3CWEMGo9orqne8jFar05_p5fKz26EZnl7T0Fd8A130_provenance.
- befree-2016 importedOn "2016-02-19" NP624199.RA2qfZ3CWEMGo9orqne8jFar05_p5fKz26EZnl7T0Fd8A130_provenance.