Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP671817.RAHS5Urj1FSA6PEdhxhh2u3lgSyd8snD4gfo7xgLdUcJg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP671817.RAHS5Urj1FSA6PEdhxhh2u3lgSyd8snD4gfo7xgLdUcJg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP671817.RAHS5Urj1FSA6PEdhxhh2u3lgSyd8snD4gfo7xgLdUcJg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP671817.RAHS5Urj1FSA6PEdhxhh2u3lgSyd8snD4gfo7xgLdUcJg130_provenance.
- NP671817.RAHS5Urj1FSA6PEdhxhh2u3lgSyd8snD4gfo7xgLdUcJg130_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." NP671817.RAHS5Urj1FSA6PEdhxhh2u3lgSyd8snD4gfo7xgLdUcJg130_provenance.
- NP671817.RAHS5Urj1FSA6PEdhxhh2u3lgSyd8snD4gfo7xgLdUcJg130_assertion evidence source_evidence_literature NP671817.RAHS5Urj1FSA6PEdhxhh2u3lgSyd8snD4gfo7xgLdUcJg130_provenance.
- NP671817.RAHS5Urj1FSA6PEdhxhh2u3lgSyd8snD4gfo7xgLdUcJg130_assertion SIO_000772 18488027 NP671817.RAHS5Urj1FSA6PEdhxhh2u3lgSyd8snD4gfo7xgLdUcJg130_provenance.
- NP671817.RAHS5Urj1FSA6PEdhxhh2u3lgSyd8snD4gfo7xgLdUcJg130_assertion wasDerivedFrom befree-2016 NP671817.RAHS5Urj1FSA6PEdhxhh2u3lgSyd8snD4gfo7xgLdUcJg130_provenance.
- NP671817.RAHS5Urj1FSA6PEdhxhh2u3lgSyd8snD4gfo7xgLdUcJg130_assertion wasGeneratedBy ECO_0000203 NP671817.RAHS5Urj1FSA6PEdhxhh2u3lgSyd8snD4gfo7xgLdUcJg130_provenance.
- befree-2016 importedOn "2016-02-19" NP671817.RAHS5Urj1FSA6PEdhxhh2u3lgSyd8snD4gfo7xgLdUcJg130_provenance.