Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP381286.RA2XVCg39fuMGwCZuegqDKMUsyuvsJ9R2daPMrmqHNOKI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP381286.RA2XVCg39fuMGwCZuegqDKMUsyuvsJ9R2daPMrmqHNOKI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP381286.RA2XVCg39fuMGwCZuegqDKMUsyuvsJ9R2daPMrmqHNOKI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP381286.RA2XVCg39fuMGwCZuegqDKMUsyuvsJ9R2daPMrmqHNOKI130_provenance.
- NP381286.RA2XVCg39fuMGwCZuegqDKMUsyuvsJ9R2daPMrmqHNOKI130_assertion description "[Frequent methylation in NEIL1 (42%) and infrequent methylation in ERCC1 (2%) and RAD23B (2%) are reported for the first time in NSCLC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP381286.RA2XVCg39fuMGwCZuegqDKMUsyuvsJ9R2daPMrmqHNOKI130_provenance.
- NP381286.RA2XVCg39fuMGwCZuegqDKMUsyuvsJ9R2daPMrmqHNOKI130_assertion evidence source_evidence_literature NP381286.RA2XVCg39fuMGwCZuegqDKMUsyuvsJ9R2daPMrmqHNOKI130_provenance.
- NP381286.RA2XVCg39fuMGwCZuegqDKMUsyuvsJ9R2daPMrmqHNOKI130_assertion SIO_000772 24569633 NP381286.RA2XVCg39fuMGwCZuegqDKMUsyuvsJ9R2daPMrmqHNOKI130_provenance.
- NP381286.RA2XVCg39fuMGwCZuegqDKMUsyuvsJ9R2daPMrmqHNOKI130_assertion wasDerivedFrom befree-20150227 NP381286.RA2XVCg39fuMGwCZuegqDKMUsyuvsJ9R2daPMrmqHNOKI130_provenance.
- NP381286.RA2XVCg39fuMGwCZuegqDKMUsyuvsJ9R2daPMrmqHNOKI130_assertion wasGeneratedBy ECO_0000203 NP381286.RA2XVCg39fuMGwCZuegqDKMUsyuvsJ9R2daPMrmqHNOKI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP381286.RA2XVCg39fuMGwCZuegqDKMUsyuvsJ9R2daPMrmqHNOKI130_provenance.