Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP707511.RAOn22x9IIManEZ0tRhHJSexSCX2Cl2XDIHcuOCrlD0T4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP707511.RAOn22x9IIManEZ0tRhHJSexSCX2Cl2XDIHcuOCrlD0T4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP707511.RAOn22x9IIManEZ0tRhHJSexSCX2Cl2XDIHcuOCrlD0T4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP707511.RAOn22x9IIManEZ0tRhHJSexSCX2Cl2XDIHcuOCrlD0T4130_provenance.
- NP707511.RAOn22x9IIManEZ0tRhHJSexSCX2Cl2XDIHcuOCrlD0T4130_assertion description "[The dysregulation of the RAS/MAPK pathway appears to be a common molecular pathogenesis of these disorders: mutations in PTPN11, KRAS, and SOS1 have been identified in patients with NS, those in KRAS, BRAF, MAP2K1, and MAP2K2 in patients with CFC syndrome, and those in HRAS mutations in Costello syndrome patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP707511.RAOn22x9IIManEZ0tRhHJSexSCX2Cl2XDIHcuOCrlD0T4130_provenance.
- NP707511.RAOn22x9IIManEZ0tRhHJSexSCX2Cl2XDIHcuOCrlD0T4130_assertion evidence source_evidence_literature NP707511.RAOn22x9IIManEZ0tRhHJSexSCX2Cl2XDIHcuOCrlD0T4130_provenance.
- NP707511.RAOn22x9IIManEZ0tRhHJSexSCX2Cl2XDIHcuOCrlD0T4130_assertion SIO_000772 20052757 NP707511.RAOn22x9IIManEZ0tRhHJSexSCX2Cl2XDIHcuOCrlD0T4130_provenance.
- NP707511.RAOn22x9IIManEZ0tRhHJSexSCX2Cl2XDIHcuOCrlD0T4130_assertion wasDerivedFrom befree-20150227 NP707511.RAOn22x9IIManEZ0tRhHJSexSCX2Cl2XDIHcuOCrlD0T4130_provenance.
- NP707511.RAOn22x9IIManEZ0tRhHJSexSCX2Cl2XDIHcuOCrlD0T4130_assertion wasGeneratedBy ECO_0000203 NP707511.RAOn22x9IIManEZ0tRhHJSexSCX2Cl2XDIHcuOCrlD0T4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP707511.RAOn22x9IIManEZ0tRhHJSexSCX2Cl2XDIHcuOCrlD0T4130_provenance.