Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP780414.RAW_UWDc5QKt5qVEojLondCuZBk0zzRwNkabOwuifx9Ek130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP780414.RAW_UWDc5QKt5qVEojLondCuZBk0zzRwNkabOwuifx9Ek130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP780414.RAW_UWDc5QKt5qVEojLondCuZBk0zzRwNkabOwuifx9Ek130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP780414.RAW_UWDc5QKt5qVEojLondCuZBk0zzRwNkabOwuifx9Ek130_provenance.
- NP780414.RAW_UWDc5QKt5qVEojLondCuZBk0zzRwNkabOwuifx9Ek130_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." NP780414.RAW_UWDc5QKt5qVEojLondCuZBk0zzRwNkabOwuifx9Ek130_provenance.
- NP780414.RAW_UWDc5QKt5qVEojLondCuZBk0zzRwNkabOwuifx9Ek130_assertion evidence source_evidence_literature NP780414.RAW_UWDc5QKt5qVEojLondCuZBk0zzRwNkabOwuifx9Ek130_provenance.
- NP780414.RAW_UWDc5QKt5qVEojLondCuZBk0zzRwNkabOwuifx9Ek130_assertion SIO_000772 11782372 NP780414.RAW_UWDc5QKt5qVEojLondCuZBk0zzRwNkabOwuifx9Ek130_provenance.
- NP780414.RAW_UWDc5QKt5qVEojLondCuZBk0zzRwNkabOwuifx9Ek130_assertion wasDerivedFrom befree-20150227 NP780414.RAW_UWDc5QKt5qVEojLondCuZBk0zzRwNkabOwuifx9Ek130_provenance.
- NP780414.RAW_UWDc5QKt5qVEojLondCuZBk0zzRwNkabOwuifx9Ek130_assertion wasGeneratedBy ECO_0000203 NP780414.RAW_UWDc5QKt5qVEojLondCuZBk0zzRwNkabOwuifx9Ek130_provenance.
- befree-20150227 importedOn "2015-02-27" NP780414.RAW_UWDc5QKt5qVEojLondCuZBk0zzRwNkabOwuifx9Ek130_provenance.