Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP598524.RAUMF8d1xhHsK8o_UIEVp_mcq53RNveZOWeTv8coVSsZc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP598524.RAUMF8d1xhHsK8o_UIEVp_mcq53RNveZOWeTv8coVSsZc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP598524.RAUMF8d1xhHsK8o_UIEVp_mcq53RNveZOWeTv8coVSsZc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP598524.RAUMF8d1xhHsK8o_UIEVp_mcq53RNveZOWeTv8coVSsZc130_provenance.
- NP598524.RAUMF8d1xhHsK8o_UIEVp_mcq53RNveZOWeTv8coVSsZc130_assertion description "[RAS mutations in codon 61 were by far the most common genetic alteration in poorly differentiated carcinomas (23% of cases), with all mutation in NRAS except one in the HRAS gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP598524.RAUMF8d1xhHsK8o_UIEVp_mcq53RNveZOWeTv8coVSsZc130_provenance.
- NP598524.RAUMF8d1xhHsK8o_UIEVp_mcq53RNveZOWeTv8coVSsZc130_assertion evidence source_evidence_literature NP598524.RAUMF8d1xhHsK8o_UIEVp_mcq53RNveZOWeTv8coVSsZc130_provenance.
- NP598524.RAUMF8d1xhHsK8o_UIEVp_mcq53RNveZOWeTv8coVSsZc130_assertion SIO_000772 19837916 NP598524.RAUMF8d1xhHsK8o_UIEVp_mcq53RNveZOWeTv8coVSsZc130_provenance.
- NP598524.RAUMF8d1xhHsK8o_UIEVp_mcq53RNveZOWeTv8coVSsZc130_assertion wasDerivedFrom befree-20150227 NP598524.RAUMF8d1xhHsK8o_UIEVp_mcq53RNveZOWeTv8coVSsZc130_provenance.
- NP598524.RAUMF8d1xhHsK8o_UIEVp_mcq53RNveZOWeTv8coVSsZc130_assertion wasGeneratedBy ECO_0000203 NP598524.RAUMF8d1xhHsK8o_UIEVp_mcq53RNveZOWeTv8coVSsZc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP598524.RAUMF8d1xhHsK8o_UIEVp_mcq53RNveZOWeTv8coVSsZc130_provenance.