Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP20529.RAc59WG4zAaXcoscv1LSdG5Uy8bPcca2ctgvNyGvBDrIQ130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP20529.RAc59WG4zAaXcoscv1LSdG5Uy8bPcca2ctgvNyGvBDrIQ130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP20529.RAc59WG4zAaXcoscv1LSdG5Uy8bPcca2ctgvNyGvBDrIQ130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP20529.RAc59WG4zAaXcoscv1LSdG5Uy8bPcca2ctgvNyGvBDrIQ130_provenance.
- ctd_human-20150221 importedOn "2015-02-21" NP20529.RAc59WG4zAaXcoscv1LSdG5Uy8bPcca2ctgvNyGvBDrIQ130_provenance.
- 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.