Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP151079.RALXtSi2doHhAt3OkvKqSx_ZmiLScIzFbI4BjaSO1iq3U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP151079.RALXtSi2doHhAt3OkvKqSx_ZmiLScIzFbI4BjaSO1iq3U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP151079.RALXtSi2doHhAt3OkvKqSx_ZmiLScIzFbI4BjaSO1iq3U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP151079.RALXtSi2doHhAt3OkvKqSx_ZmiLScIzFbI4BjaSO1iq3U130_provenance.
- NP151079.RALXtSi2doHhAt3OkvKqSx_ZmiLScIzFbI4BjaSO1iq3U130_assertion description "[Overall, the XRCC1 homozygous variant gln399gln genotype was related to a significantly reduced risk of both basal cell BCC; odds ratio (OR) 0.7, 95% confidence interval 0.4-1.0 and squamous cell carcinoma (SCC; OR 0.6, 95% confidence interval 0.3-0.9).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP151079.RALXtSi2doHhAt3OkvKqSx_ZmiLScIzFbI4BjaSO1iq3U130_provenance.
- NP151079.RALXtSi2doHhAt3OkvKqSx_ZmiLScIzFbI4BjaSO1iq3U130_assertion evidence source_evidence_literature NP151079.RALXtSi2doHhAt3OkvKqSx_ZmiLScIzFbI4BjaSO1iq3U130_provenance.
- NP151079.RALXtSi2doHhAt3OkvKqSx_ZmiLScIzFbI4BjaSO1iq3U130_assertion SIO_000772 11782372 NP151079.RALXtSi2doHhAt3OkvKqSx_ZmiLScIzFbI4BjaSO1iq3U130_provenance.
- NP151079.RALXtSi2doHhAt3OkvKqSx_ZmiLScIzFbI4BjaSO1iq3U130_assertion wasDerivedFrom gad-20150221 NP151079.RALXtSi2doHhAt3OkvKqSx_ZmiLScIzFbI4BjaSO1iq3U130_provenance.
- NP151079.RALXtSi2doHhAt3OkvKqSx_ZmiLScIzFbI4BjaSO1iq3U130_assertion wasGeneratedBy ECO_0000203 NP151079.RALXtSi2doHhAt3OkvKqSx_ZmiLScIzFbI4BjaSO1iq3U130_provenance.
- gad-20150221 importedOn "2015-02-21" NP151079.RALXtSi2doHhAt3OkvKqSx_ZmiLScIzFbI4BjaSO1iq3U130_provenance.