Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP671809.RAc4vQJAXTmsbexflK7R_1qKha9dGxOCcUoQg_klQQuD0130_assertion> ?p ?o ?g. }
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- NP671809.RAc4vQJAXTmsbexflK7R_1qKha9dGxOCcUoQg_klQQuD0130_assertion type Assertion NP671809.RAc4vQJAXTmsbexflK7R_1qKha9dGxOCcUoQg_klQQuD0130_head.
- NP671809.RAc4vQJAXTmsbexflK7R_1qKha9dGxOCcUoQg_klQQuD0130_assertion description "[A haplotype near ASIP, known to affect a similar spectrum of pigmentation traits as MC1R variants, conferred significant risk of CM (odds ratio (OR) = 1.45, P = 1.2 x 10(-9)) and BCC (OR = 1.33, P = 1.2 x 10(-6)).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP671809.RAc4vQJAXTmsbexflK7R_1qKha9dGxOCcUoQg_klQQuD0130_provenance.
- NP671809.RAc4vQJAXTmsbexflK7R_1qKha9dGxOCcUoQg_klQQuD0130_assertion evidence source_evidence_literature NP671809.RAc4vQJAXTmsbexflK7R_1qKha9dGxOCcUoQg_klQQuD0130_provenance.
- NP671809.RAc4vQJAXTmsbexflK7R_1qKha9dGxOCcUoQg_klQQuD0130_assertion SIO_000772 18488027 NP671809.RAc4vQJAXTmsbexflK7R_1qKha9dGxOCcUoQg_klQQuD0130_provenance.
- NP671809.RAc4vQJAXTmsbexflK7R_1qKha9dGxOCcUoQg_klQQuD0130_assertion wasDerivedFrom befree-2016 NP671809.RAc4vQJAXTmsbexflK7R_1qKha9dGxOCcUoQg_klQQuD0130_provenance.
- NP671809.RAc4vQJAXTmsbexflK7R_1qKha9dGxOCcUoQg_klQQuD0130_assertion wasGeneratedBy ECO_0000203 NP671809.RAc4vQJAXTmsbexflK7R_1qKha9dGxOCcUoQg_klQQuD0130_provenance.