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- source_evidence_literature type ECO_0000212 NP68985.RAnpVcQHbYwhXGlj6metVQAp1W-8Fwmyhs3MlQt2ssT-U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP68985.RAnpVcQHbYwhXGlj6metVQAp1W-8Fwmyhs3MlQt2ssT-U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP68985.RAnpVcQHbYwhXGlj6metVQAp1W-8Fwmyhs3MlQt2ssT-U130_provenance.
- NP68985.RAnpVcQHbYwhXGlj6metVQAp1W-8Fwmyhs3MlQt2ssT-U130_assertion description "[A non-synonymous SNP in the MC1R gene (rs1805007 encoding Arg151Cys substitution), a previously well-documented pigmentation gene, showed the strongest association with BCC risk in the discovery set (rs1805007T: OR (95% CI) for combined discovery set and replication set 1.55 (1.45-1.66); P= 4.3 A 10(-17).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP68985.RAnpVcQHbYwhXGlj6metVQAp1W-8Fwmyhs3MlQt2ssT-U130_provenance.
- NP68985.RAnpVcQHbYwhXGlj6metVQAp1W-8Fwmyhs3MlQt2ssT-U130_assertion evidence source_evidence_literature NP68985.RAnpVcQHbYwhXGlj6metVQAp1W-8Fwmyhs3MlQt2ssT-U130_provenance.
- NP68985.RAnpVcQHbYwhXGlj6metVQAp1W-8Fwmyhs3MlQt2ssT-U130_assertion SIO_000772 21700618 NP68985.RAnpVcQHbYwhXGlj6metVQAp1W-8Fwmyhs3MlQt2ssT-U130_provenance.
- NP68985.RAnpVcQHbYwhXGlj6metVQAp1W-8Fwmyhs3MlQt2ssT-U130_assertion wasDerivedFrom gad-20150221 NP68985.RAnpVcQHbYwhXGlj6metVQAp1W-8Fwmyhs3MlQt2ssT-U130_provenance.
- NP68985.RAnpVcQHbYwhXGlj6metVQAp1W-8Fwmyhs3MlQt2ssT-U130_assertion wasGeneratedBy ECO_0000203 NP68985.RAnpVcQHbYwhXGlj6metVQAp1W-8Fwmyhs3MlQt2ssT-U130_provenance.
- gad-20150221 importedOn "2015-02-21" NP68985.RAnpVcQHbYwhXGlj6metVQAp1W-8Fwmyhs3MlQt2ssT-U130_provenance.