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- source_evidence_literature type ECO_0000212 NP607349.RA1331nm1rD8TNvHGg81HM0DkbiV6UM0VN16pY_GO3qsE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP607349.RA1331nm1rD8TNvHGg81HM0DkbiV6UM0VN16pY_GO3qsE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP607349.RA1331nm1rD8TNvHGg81HM0DkbiV6UM0VN16pY_GO3qsE130_provenance.
- befree-2016 importedOn "2016-02-19" NP607349.RA1331nm1rD8TNvHGg81HM0DkbiV6UM0VN16pY_GO3qsE130_provenance.
- NP607349.RA1331nm1rD8TNvHGg81HM0DkbiV6UM0VN16pY_GO3qsE130_assertion wasGeneratedBy ECO_0000203 NP607349.RA1331nm1rD8TNvHGg81HM0DkbiV6UM0VN16pY_GO3qsE130_provenance.
- NP607349.RA1331nm1rD8TNvHGg81HM0DkbiV6UM0VN16pY_GO3qsE130_assertion wasDerivedFrom befree-2016 NP607349.RA1331nm1rD8TNvHGg81HM0DkbiV6UM0VN16pY_GO3qsE130_provenance.
- NP607349.RA1331nm1rD8TNvHGg81HM0DkbiV6UM0VN16pY_GO3qsE130_assertion SIO_000772 17468812 NP607349.RA1331nm1rD8TNvHGg81HM0DkbiV6UM0VN16pY_GO3qsE130_provenance.
- NP607349.RA1331nm1rD8TNvHGg81HM0DkbiV6UM0VN16pY_GO3qsE130_assertion evidence source_evidence_literature NP607349.RA1331nm1rD8TNvHGg81HM0DkbiV6UM0VN16pY_GO3qsE130_provenance.
- NP607349.RA1331nm1rD8TNvHGg81HM0DkbiV6UM0VN16pY_GO3qsE130_assertion description "[We report on a novel KRAS gene mutation in a patient presenting the clinical features typical of Costello syndrome and the additional findings seen in Noonan syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP607349.RA1331nm1rD8TNvHGg81HM0DkbiV6UM0VN16pY_GO3qsE130_provenance.