Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP305462.RA0f5uw8uguE-1VUvIkfBLC7jZidrDlYPKSnSoaJP5SWo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP305462.RA0f5uw8uguE-1VUvIkfBLC7jZidrDlYPKSnSoaJP5SWo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP305462.RA0f5uw8uguE-1VUvIkfBLC7jZidrDlYPKSnSoaJP5SWo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP305462.RA0f5uw8uguE-1VUvIkfBLC7jZidrDlYPKSnSoaJP5SWo130_provenance.
- NP305462.RA0f5uw8uguE-1VUvIkfBLC7jZidrDlYPKSnSoaJP5SWo130_assertion description "[Among patients with melanoma genetically tested, CDKN2A G101W mutation carriers were more frequently younger (P�=�0.023), with clinically atypical nevi (P�=�0.050), with cytological atypia (P�=�0.033) at confocal.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP305462.RA0f5uw8uguE-1VUvIkfBLC7jZidrDlYPKSnSoaJP5SWo130_provenance.
- NP305462.RA0f5uw8uguE-1VUvIkfBLC7jZidrDlYPKSnSoaJP5SWo130_assertion evidence source_evidence_literature NP305462.RA0f5uw8uguE-1VUvIkfBLC7jZidrDlYPKSnSoaJP5SWo130_provenance.
- NP305462.RA0f5uw8uguE-1VUvIkfBLC7jZidrDlYPKSnSoaJP5SWo130_assertion SIO_000772 23711066 NP305462.RA0f5uw8uguE-1VUvIkfBLC7jZidrDlYPKSnSoaJP5SWo130_provenance.
- NP305462.RA0f5uw8uguE-1VUvIkfBLC7jZidrDlYPKSnSoaJP5SWo130_assertion wasDerivedFrom befree-20150227 NP305462.RA0f5uw8uguE-1VUvIkfBLC7jZidrDlYPKSnSoaJP5SWo130_provenance.
- NP305462.RA0f5uw8uguE-1VUvIkfBLC7jZidrDlYPKSnSoaJP5SWo130_assertion wasGeneratedBy ECO_0000203 NP305462.RA0f5uw8uguE-1VUvIkfBLC7jZidrDlYPKSnSoaJP5SWo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP305462.RA0f5uw8uguE-1VUvIkfBLC7jZidrDlYPKSnSoaJP5SWo130_provenance.