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- source_evidence_literature type ECO_0000212 NP575617.RAk__uNey1_ejsBZu3GCYxrA8YjyrusCwrK64FaLrA6z0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP575617.RAk__uNey1_ejsBZu3GCYxrA8YjyrusCwrK64FaLrA6z0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP575617.RAk__uNey1_ejsBZu3GCYxrA8YjyrusCwrK64FaLrA6z0130_provenance.
- befree-2016 importedOn "2016-02-19" NP575617.RAk__uNey1_ejsBZu3GCYxrA8YjyrusCwrK64FaLrA6z0130_provenance.
- NP575617.RAk__uNey1_ejsBZu3GCYxrA8YjyrusCwrK64FaLrA6z0130_assertion wasGeneratedBy ECO_0000203 NP575617.RAk__uNey1_ejsBZu3GCYxrA8YjyrusCwrK64FaLrA6z0130_provenance.
- NP575617.RAk__uNey1_ejsBZu3GCYxrA8YjyrusCwrK64FaLrA6z0130_assertion wasDerivedFrom befree-2016 NP575617.RAk__uNey1_ejsBZu3GCYxrA8YjyrusCwrK64FaLrA6z0130_provenance.
- NP575617.RAk__uNey1_ejsBZu3GCYxrA8YjyrusCwrK64FaLrA6z0130_assertion SIO_000772 17056636 NP575617.RAk__uNey1_ejsBZu3GCYxrA8YjyrusCwrK64FaLrA6z0130_provenance.
- NP575617.RAk__uNey1_ejsBZu3GCYxrA8YjyrusCwrK64FaLrA6z0130_assertion evidence source_evidence_literature NP575617.RAk__uNey1_ejsBZu3GCYxrA8YjyrusCwrK64FaLrA6z0130_provenance.
- NP575617.RAk__uNey1_ejsBZu3GCYxrA8YjyrusCwrK64FaLrA6z0130_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." NP575617.RAk__uNey1_ejsBZu3GCYxrA8YjyrusCwrK64FaLrA6z0130_provenance.