Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP948637.RAXvsJVX67s4V8NrstIordcIE2b-v2Qv-3g5xnFG8y9HQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP948637.RAXvsJVX67s4V8NrstIordcIE2b-v2Qv-3g5xnFG8y9HQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP948637.RAXvsJVX67s4V8NrstIordcIE2b-v2Qv-3g5xnFG8y9HQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP948637.RAXvsJVX67s4V8NrstIordcIE2b-v2Qv-3g5xnFG8y9HQ130_provenance.
- NP948637.RAXvsJVX67s4V8NrstIordcIE2b-v2Qv-3g5xnFG8y9HQ130_assertion description "[MC1R variants increased the risk of sporadic cutaneous melanoma in darker-pigmented Caucasians: a pooled-analysis from the M-SKIP project.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP948637.RAXvsJVX67s4V8NrstIordcIE2b-v2Qv-3g5xnFG8y9HQ130_provenance.
- NP948637.RAXvsJVX67s4V8NrstIordcIE2b-v2Qv-3g5xnFG8y9HQ130_assertion evidence source_evidence_literature NP948637.RAXvsJVX67s4V8NrstIordcIE2b-v2Qv-3g5xnFG8y9HQ130_provenance.
- NP948637.RAXvsJVX67s4V8NrstIordcIE2b-v2Qv-3g5xnFG8y9HQ130_assertion SIO_000772 24917043 NP948637.RAXvsJVX67s4V8NrstIordcIE2b-v2Qv-3g5xnFG8y9HQ130_provenance.
- NP948637.RAXvsJVX67s4V8NrstIordcIE2b-v2Qv-3g5xnFG8y9HQ130_assertion wasDerivedFrom befree-20150227 NP948637.RAXvsJVX67s4V8NrstIordcIE2b-v2Qv-3g5xnFG8y9HQ130_provenance.
- NP948637.RAXvsJVX67s4V8NrstIordcIE2b-v2Qv-3g5xnFG8y9HQ130_assertion wasGeneratedBy ECO_0000203 NP948637.RAXvsJVX67s4V8NrstIordcIE2b-v2Qv-3g5xnFG8y9HQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP948637.RAXvsJVX67s4V8NrstIordcIE2b-v2Qv-3g5xnFG8y9HQ130_provenance.