Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP829868.RA8S8WEXaR7kxqi_hn5MZCzsP_wsgvFGCYuVzDntj8dk0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP829868.RA8S8WEXaR7kxqi_hn5MZCzsP_wsgvFGCYuVzDntj8dk0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP829868.RA8S8WEXaR7kxqi_hn5MZCzsP_wsgvFGCYuVzDntj8dk0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP829868.RA8S8WEXaR7kxqi_hn5MZCzsP_wsgvFGCYuVzDntj8dk0130_provenance.
- NP829868.RA8S8WEXaR7kxqi_hn5MZCzsP_wsgvFGCYuVzDntj8dk0130_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 (rs1805007[T]: OR (95% CI) for combined discovery set and replication set [1.55 (1.45-1.66); P= 4.3 � 10(-17)].]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP829868.RA8S8WEXaR7kxqi_hn5MZCzsP_wsgvFGCYuVzDntj8dk0130_provenance.
- NP829868.RA8S8WEXaR7kxqi_hn5MZCzsP_wsgvFGCYuVzDntj8dk0130_assertion evidence source_evidence_literature NP829868.RA8S8WEXaR7kxqi_hn5MZCzsP_wsgvFGCYuVzDntj8dk0130_provenance.
- NP829868.RA8S8WEXaR7kxqi_hn5MZCzsP_wsgvFGCYuVzDntj8dk0130_assertion SIO_000772 21700618 NP829868.RA8S8WEXaR7kxqi_hn5MZCzsP_wsgvFGCYuVzDntj8dk0130_provenance.
- NP829868.RA8S8WEXaR7kxqi_hn5MZCzsP_wsgvFGCYuVzDntj8dk0130_assertion wasDerivedFrom befree-20150227 NP829868.RA8S8WEXaR7kxqi_hn5MZCzsP_wsgvFGCYuVzDntj8dk0130_provenance.
- NP829868.RA8S8WEXaR7kxqi_hn5MZCzsP_wsgvFGCYuVzDntj8dk0130_assertion wasGeneratedBy ECO_0000203 NP829868.RA8S8WEXaR7kxqi_hn5MZCzsP_wsgvFGCYuVzDntj8dk0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP829868.RA8S8WEXaR7kxqi_hn5MZCzsP_wsgvFGCYuVzDntj8dk0130_provenance.