Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1265688.RAT1iORKRNPL75-wBkpBA3o39TnQ5chK4pzsLI2x4NwtY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1265688.RAT1iORKRNPL75-wBkpBA3o39TnQ5chK4pzsLI2x4NwtY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1265688.RAT1iORKRNPL75-wBkpBA3o39TnQ5chK4pzsLI2x4NwtY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1265688.RAT1iORKRNPL75-wBkpBA3o39TnQ5chK4pzsLI2x4NwtY130_provenance.
- NP1265688.RAT1iORKRNPL75-wBkpBA3o39TnQ5chK4pzsLI2x4NwtY130_assertion description "[Mutations in RAF1 are associated with Noonan syndrome and hypertrophic cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1265688.RAT1iORKRNPL75-wBkpBA3o39TnQ5chK4pzsLI2x4NwtY130_provenance.
- NP1265688.RAT1iORKRNPL75-wBkpBA3o39TnQ5chK4pzsLI2x4NwtY130_assertion evidence source_evidence_literature NP1265688.RAT1iORKRNPL75-wBkpBA3o39TnQ5chK4pzsLI2x4NwtY130_provenance.
- NP1265688.RAT1iORKRNPL75-wBkpBA3o39TnQ5chK4pzsLI2x4NwtY130_assertion SIO_000772 25706034 NP1265688.RAT1iORKRNPL75-wBkpBA3o39TnQ5chK4pzsLI2x4NwtY130_provenance.
- NP1265688.RAT1iORKRNPL75-wBkpBA3o39TnQ5chK4pzsLI2x4NwtY130_assertion wasDerivedFrom befree-2016 NP1265688.RAT1iORKRNPL75-wBkpBA3o39TnQ5chK4pzsLI2x4NwtY130_provenance.
- NP1265688.RAT1iORKRNPL75-wBkpBA3o39TnQ5chK4pzsLI2x4NwtY130_assertion wasGeneratedBy ECO_0000203 NP1265688.RAT1iORKRNPL75-wBkpBA3o39TnQ5chK4pzsLI2x4NwtY130_provenance.
- befree-2016 importedOn "2016-02-19" NP1265688.RAT1iORKRNPL75-wBkpBA3o39TnQ5chK4pzsLI2x4NwtY130_provenance.