Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP341558.RAR1HkhM0eLYBsYHwo69q6JuFv-3YReObVPiaZ4O3SNwc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP341558.RAR1HkhM0eLYBsYHwo69q6JuFv-3YReObVPiaZ4O3SNwc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP341558.RAR1HkhM0eLYBsYHwo69q6JuFv-3YReObVPiaZ4O3SNwc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP341558.RAR1HkhM0eLYBsYHwo69q6JuFv-3YReObVPiaZ4O3SNwc130_provenance.
- NP341558.RAR1HkhM0eLYBsYHwo69q6JuFv-3YReObVPiaZ4O3SNwc130_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." NP341558.RAR1HkhM0eLYBsYHwo69q6JuFv-3YReObVPiaZ4O3SNwc130_provenance.
- NP341558.RAR1HkhM0eLYBsYHwo69q6JuFv-3YReObVPiaZ4O3SNwc130_assertion evidence source_evidence_literature NP341558.RAR1HkhM0eLYBsYHwo69q6JuFv-3YReObVPiaZ4O3SNwc130_provenance.
- NP341558.RAR1HkhM0eLYBsYHwo69q6JuFv-3YReObVPiaZ4O3SNwc130_assertion SIO_000772 11782372 NP341558.RAR1HkhM0eLYBsYHwo69q6JuFv-3YReObVPiaZ4O3SNwc130_provenance.
- NP341558.RAR1HkhM0eLYBsYHwo69q6JuFv-3YReObVPiaZ4O3SNwc130_assertion wasDerivedFrom befree-2016 NP341558.RAR1HkhM0eLYBsYHwo69q6JuFv-3YReObVPiaZ4O3SNwc130_provenance.
- NP341558.RAR1HkhM0eLYBsYHwo69q6JuFv-3YReObVPiaZ4O3SNwc130_assertion wasGeneratedBy ECO_0000203 NP341558.RAR1HkhM0eLYBsYHwo69q6JuFv-3YReObVPiaZ4O3SNwc130_provenance.
- befree-2016 importedOn "2016-02-19" NP341558.RAR1HkhM0eLYBsYHwo69q6JuFv-3YReObVPiaZ4O3SNwc130_provenance.