Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP4159.RAJxoqY-snNvHGTGjF-LIt6YY9B47dkb4MfQnIg4UhjVM130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP4159.RAJxoqY-snNvHGTGjF-LIt6YY9B47dkb4MfQnIg4UhjVM130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP4159.RAJxoqY-snNvHGTGjF-LIt6YY9B47dkb4MfQnIg4UhjVM130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP4159.RAJxoqY-snNvHGTGjF-LIt6YY9B47dkb4MfQnIg4UhjVM130_provenance.
- NP4159.RAJxoqY-snNvHGTGjF-LIt6YY9B47dkb4MfQnIg4UhjVM130_assertion description "[MSH2 missense mutations and HNPCC syndrome: pathogenicity assessment in a human expression system.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP4159.RAJxoqY-snNvHGTGjF-LIt6YY9B47dkb4MfQnIg4UhjVM130_provenance.
- NP4159.RAJxoqY-snNvHGTGjF-LIt6YY9B47dkb4MfQnIg4UhjVM130_assertion evidence source_evidence_curated NP4159.RAJxoqY-snNvHGTGjF-LIt6YY9B47dkb4MfQnIg4UhjVM130_provenance.
- NP4159.RAJxoqY-snNvHGTGjF-LIt6YY9B47dkb4MfQnIg4UhjVM130_assertion SIO_000772 18781619 NP4159.RAJxoqY-snNvHGTGjF-LIt6YY9B47dkb4MfQnIg4UhjVM130_provenance.
- NP4159.RAJxoqY-snNvHGTGjF-LIt6YY9B47dkb4MfQnIg4UhjVM130_assertion wasDerivedFrom uniprot-20130724 NP4159.RAJxoqY-snNvHGTGjF-LIt6YY9B47dkb4MfQnIg4UhjVM130_provenance.
- NP4159.RAJxoqY-snNvHGTGjF-LIt6YY9B47dkb4MfQnIg4UhjVM130_assertion wasGeneratedBy ECO_0000218 NP4159.RAJxoqY-snNvHGTGjF-LIt6YY9B47dkb4MfQnIg4UhjVM130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP4159.RAJxoqY-snNvHGTGjF-LIt6YY9B47dkb4MfQnIg4UhjVM130_provenance.