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- source_evidence_literature type ECO_0000212 NP575616.RA6CzY4BBenvmYOPNudc9509-RoZg4Pf5G48LVuGwZ99s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP575616.RA6CzY4BBenvmYOPNudc9509-RoZg4Pf5G48LVuGwZ99s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP575616.RA6CzY4BBenvmYOPNudc9509-RoZg4Pf5G48LVuGwZ99s130_provenance.
- befree-2016 importedOn "2016-02-19" NP575616.RA6CzY4BBenvmYOPNudc9509-RoZg4Pf5G48LVuGwZ99s130_provenance.
- NP575616.RA6CzY4BBenvmYOPNudc9509-RoZg4Pf5G48LVuGwZ99s130_assertion wasGeneratedBy ECO_0000203 NP575616.RA6CzY4BBenvmYOPNudc9509-RoZg4Pf5G48LVuGwZ99s130_provenance.
- NP575616.RA6CzY4BBenvmYOPNudc9509-RoZg4Pf5G48LVuGwZ99s130_assertion wasDerivedFrom befree-2016 NP575616.RA6CzY4BBenvmYOPNudc9509-RoZg4Pf5G48LVuGwZ99s130_provenance.
- NP575616.RA6CzY4BBenvmYOPNudc9509-RoZg4Pf5G48LVuGwZ99s130_assertion SIO_000772 17056636 NP575616.RA6CzY4BBenvmYOPNudc9509-RoZg4Pf5G48LVuGwZ99s130_provenance.
- NP575616.RA6CzY4BBenvmYOPNudc9509-RoZg4Pf5G48LVuGwZ99s130_assertion evidence source_evidence_literature NP575616.RA6CzY4BBenvmYOPNudc9509-RoZg4Pf5G48LVuGwZ99s130_provenance.
- NP575616.RA6CzY4BBenvmYOPNudc9509-RoZg4Pf5G48LVuGwZ99s130_assertion description "[Remarkably, our cohort of individuals with KRAS mutations showed a high clinical variability, ranging from Noonan syndrome to CFC, and also included two patients who met the clinical criteria of Costello syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP575616.RA6CzY4BBenvmYOPNudc9509-RoZg4Pf5G48LVuGwZ99s130_provenance.