Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP830518.RAS68IrQndWNx7zX0iFWWdZEBpAO_8z9iKKVxqAKiBclA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP830518.RAS68IrQndWNx7zX0iFWWdZEBpAO_8z9iKKVxqAKiBclA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP830518.RAS68IrQndWNx7zX0iFWWdZEBpAO_8z9iKKVxqAKiBclA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP830518.RAS68IrQndWNx7zX0iFWWdZEBpAO_8z9iKKVxqAKiBclA130_provenance.
- NP830518.RAS68IrQndWNx7zX0iFWWdZEBpAO_8z9iKKVxqAKiBclA130_assertion description "[We found missense mutations of AAC (Asn) to AGC (Ser) at DCC codon 176 in one cell line and ACC (Thr) to ATC (Ile) at codon 1105 in one cell line and tumor, respectively; polymorphisms of CGA (Arg) to GGA (Gly) at codon 201 and TTT (Phe) to TTG (Leu) at codon 951 in most of the cell lines and tumors; and a silent mutation of GAG (Glu) to GAA (Glu) at codon 118 in four cell lines and five primary tumors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP830518.RAS68IrQndWNx7zX0iFWWdZEBpAO_8z9iKKVxqAKiBclA130_provenance.
- NP830518.RAS68IrQndWNx7zX0iFWWdZEBpAO_8z9iKKVxqAKiBclA130_assertion evidence source_evidence_literature NP830518.RAS68IrQndWNx7zX0iFWWdZEBpAO_8z9iKKVxqAKiBclA130_provenance.
- NP830518.RAS68IrQndWNx7zX0iFWWdZEBpAO_8z9iKKVxqAKiBclA130_assertion SIO_000772 9288786 NP830518.RAS68IrQndWNx7zX0iFWWdZEBpAO_8z9iKKVxqAKiBclA130_provenance.
- NP830518.RAS68IrQndWNx7zX0iFWWdZEBpAO_8z9iKKVxqAKiBclA130_assertion wasDerivedFrom befree-20150227 NP830518.RAS68IrQndWNx7zX0iFWWdZEBpAO_8z9iKKVxqAKiBclA130_provenance.
- NP830518.RAS68IrQndWNx7zX0iFWWdZEBpAO_8z9iKKVxqAKiBclA130_assertion wasGeneratedBy ECO_0000203 NP830518.RAS68IrQndWNx7zX0iFWWdZEBpAO_8z9iKKVxqAKiBclA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP830518.RAS68IrQndWNx7zX0iFWWdZEBpAO_8z9iKKVxqAKiBclA130_provenance.