Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP20529.RAc59WG4zAaXcoscv1LSdG5Uy8bPcca2ctgvNyGvBDrIQ130_assertion> ?p ?o ?g. }
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- NP20529.RAc59WG4zAaXcoscv1LSdG5Uy8bPcca2ctgvNyGvBDrIQ130_assertion type Assertion NP20529.RAc59WG4zAaXcoscv1LSdG5Uy8bPcca2ctgvNyGvBDrIQ130_head.
- NP20529.RAc59WG4zAaXcoscv1LSdG5Uy8bPcca2ctgvNyGvBDrIQ130_assertion wasGeneratedBy ECO_0000218 NP20529.RAc59WG4zAaXcoscv1LSdG5Uy8bPcca2ctgvNyGvBDrIQ130_provenance.
- NP20529.RAc59WG4zAaXcoscv1LSdG5Uy8bPcca2ctgvNyGvBDrIQ130_assertion wasDerivedFrom ctd_human-20150221 NP20529.RAc59WG4zAaXcoscv1LSdG5Uy8bPcca2ctgvNyGvBDrIQ130_provenance.
- NP20529.RAc59WG4zAaXcoscv1LSdG5Uy8bPcca2ctgvNyGvBDrIQ130_assertion SIO_000772 17468812 NP20529.RAc59WG4zAaXcoscv1LSdG5Uy8bPcca2ctgvNyGvBDrIQ130_provenance.
- NP20529.RAc59WG4zAaXcoscv1LSdG5Uy8bPcca2ctgvNyGvBDrIQ130_assertion evidence source_evidence_curated NP20529.RAc59WG4zAaXcoscv1LSdG5Uy8bPcca2ctgvNyGvBDrIQ130_provenance.
- NP20529.RAc59WG4zAaXcoscv1LSdG5Uy8bPcca2ctgvNyGvBDrIQ130_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." NP20529.RAc59WG4zAaXcoscv1LSdG5Uy8bPcca2ctgvNyGvBDrIQ130_provenance.