Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP490288.RAuNlvSxizuJbjDrJsRg4hK-_wuOWENMuFGAgPtHspMz0130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP490288.RAuNlvSxizuJbjDrJsRg4hK-_wuOWENMuFGAgPtHspMz0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP490288.RAuNlvSxizuJbjDrJsRg4hK-_wuOWENMuFGAgPtHspMz0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP490288.RAuNlvSxizuJbjDrJsRg4hK-_wuOWENMuFGAgPtHspMz0130_provenance.
- NP490288.RAuNlvSxizuJbjDrJsRg4hK-_wuOWENMuFGAgPtHspMz0130_assertion wasGeneratedBy ECO_0000203 NP490288.RAuNlvSxizuJbjDrJsRg4hK-_wuOWENMuFGAgPtHspMz0130_provenance.
- NP490288.RAuNlvSxizuJbjDrJsRg4hK-_wuOWENMuFGAgPtHspMz0130_assertion wasDerivedFrom befree-20140225 NP490288.RAuNlvSxizuJbjDrJsRg4hK-_wuOWENMuFGAgPtHspMz0130_provenance.
- NP490288.RAuNlvSxizuJbjDrJsRg4hK-_wuOWENMuFGAgPtHspMz0130_assertion SIO_000772 17056636 NP490288.RAuNlvSxizuJbjDrJsRg4hK-_wuOWENMuFGAgPtHspMz0130_provenance.
- NP490288.RAuNlvSxizuJbjDrJsRg4hK-_wuOWENMuFGAgPtHspMz0130_assertion evidence source_evidence_literature NP490288.RAuNlvSxizuJbjDrJsRg4hK-_wuOWENMuFGAgPtHspMz0130_provenance.
- NP490288.RAuNlvSxizuJbjDrJsRg4hK-_wuOWENMuFGAgPtHspMz0130_assertion description "[We further defined the phenotypic spectrum associated with KRAS missense mutations and provided the first evidence of clinical differences in patients with KRAS mutations compared with Noonan syndrome affected individuals with heterozygous PTPN11 mutations and CFC patients carrying a BRAF, MEK1 or MEK1 alteration, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP490288.RAuNlvSxizuJbjDrJsRg4hK-_wuOWENMuFGAgPtHspMz0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP490288.RAuNlvSxizuJbjDrJsRg4hK-_wuOWENMuFGAgPtHspMz0130_provenance.