Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP773.RAUT0tzmDSzb2i9143GNxaAkA9_9YBCLFCc_QIdxHaruI130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP773.RAUT0tzmDSzb2i9143GNxaAkA9_9YBCLFCc_QIdxHaruI130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP773.RAUT0tzmDSzb2i9143GNxaAkA9_9YBCLFCc_QIdxHaruI130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP773.RAUT0tzmDSzb2i9143GNxaAkA9_9YBCLFCc_QIdxHaruI130_provenance.
- NP773.RAUT0tzmDSzb2i9143GNxaAkA9_9YBCLFCc_QIdxHaruI130_assertion description "[Germline BRAF mutations in Noonan, LEOPARD, and cardiofaciocutaneous syndromes: molecular diversity and associated phenotypic spectrum.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP773.RAUT0tzmDSzb2i9143GNxaAkA9_9YBCLFCc_QIdxHaruI130_provenance.
- NP773.RAUT0tzmDSzb2i9143GNxaAkA9_9YBCLFCc_QIdxHaruI130_assertion evidence source_evidence_curated NP773.RAUT0tzmDSzb2i9143GNxaAkA9_9YBCLFCc_QIdxHaruI130_provenance.
- NP773.RAUT0tzmDSzb2i9143GNxaAkA9_9YBCLFCc_QIdxHaruI130_assertion SIO_000772 19206169 NP773.RAUT0tzmDSzb2i9143GNxaAkA9_9YBCLFCc_QIdxHaruI130_provenance.
- NP773.RAUT0tzmDSzb2i9143GNxaAkA9_9YBCLFCc_QIdxHaruI130_assertion wasDerivedFrom uniprot-20130724 NP773.RAUT0tzmDSzb2i9143GNxaAkA9_9YBCLFCc_QIdxHaruI130_provenance.
- NP773.RAUT0tzmDSzb2i9143GNxaAkA9_9YBCLFCc_QIdxHaruI130_assertion wasGeneratedBy ECO_0000218 NP773.RAUT0tzmDSzb2i9143GNxaAkA9_9YBCLFCc_QIdxHaruI130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP773.RAUT0tzmDSzb2i9143GNxaAkA9_9YBCLFCc_QIdxHaruI130_provenance.