Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP739533.RAO8Z2Fa-LOV5z3hwEr7b9c6xukWZeY3wzBMrOhPTjbjc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP739533.RAO8Z2Fa-LOV5z3hwEr7b9c6xukWZeY3wzBMrOhPTjbjc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP739533.RAO8Z2Fa-LOV5z3hwEr7b9c6xukWZeY3wzBMrOhPTjbjc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP739533.RAO8Z2Fa-LOV5z3hwEr7b9c6xukWZeY3wzBMrOhPTjbjc130_provenance.
- NP739533.RAO8Z2Fa-LOV5z3hwEr7b9c6xukWZeY3wzBMrOhPTjbjc130_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." NP739533.RAO8Z2Fa-LOV5z3hwEr7b9c6xukWZeY3wzBMrOhPTjbjc130_provenance.
- NP739533.RAO8Z2Fa-LOV5z3hwEr7b9c6xukWZeY3wzBMrOhPTjbjc130_assertion evidence source_evidence_literature NP739533.RAO8Z2Fa-LOV5z3hwEr7b9c6xukWZeY3wzBMrOhPTjbjc130_provenance.
- NP739533.RAO8Z2Fa-LOV5z3hwEr7b9c6xukWZeY3wzBMrOhPTjbjc130_assertion SIO_000772 11782372 NP739533.RAO8Z2Fa-LOV5z3hwEr7b9c6xukWZeY3wzBMrOhPTjbjc130_provenance.
- NP739533.RAO8Z2Fa-LOV5z3hwEr7b9c6xukWZeY3wzBMrOhPTjbjc130_assertion wasDerivedFrom befree-20140225 NP739533.RAO8Z2Fa-LOV5z3hwEr7b9c6xukWZeY3wzBMrOhPTjbjc130_provenance.
- NP739533.RAO8Z2Fa-LOV5z3hwEr7b9c6xukWZeY3wzBMrOhPTjbjc130_assertion wasGeneratedBy ECO_0000203 NP739533.RAO8Z2Fa-LOV5z3hwEr7b9c6xukWZeY3wzBMrOhPTjbjc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP739533.RAO8Z2Fa-LOV5z3hwEr7b9c6xukWZeY3wzBMrOhPTjbjc130_provenance.