Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP673037.RASXOYLOywf6m7H99SSP4rdCd3N8WGVLNQ3MWvVRgS3R4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP673037.RASXOYLOywf6m7H99SSP4rdCd3N8WGVLNQ3MWvVRgS3R4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP673037.RASXOYLOywf6m7H99SSP4rdCd3N8WGVLNQ3MWvVRgS3R4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP673037.RASXOYLOywf6m7H99SSP4rdCd3N8WGVLNQ3MWvVRgS3R4130_provenance.
- NP673037.RASXOYLOywf6m7H99SSP4rdCd3N8WGVLNQ3MWvVRgS3R4130_assertion description "[This article provides evidence of the wide clinical spectrum of cancer susceptibility associated with a BAP1 germline mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP673037.RASXOYLOywf6m7H99SSP4rdCd3N8WGVLNQ3MWvVRgS3R4130_provenance.
- NP673037.RASXOYLOywf6m7H99SSP4rdCd3N8WGVLNQ3MWvVRgS3R4130_assertion evidence source_evidence_literature NP673037.RASXOYLOywf6m7H99SSP4rdCd3N8WGVLNQ3MWvVRgS3R4130_provenance.
- NP673037.RASXOYLOywf6m7H99SSP4rdCd3N8WGVLNQ3MWvVRgS3R4130_assertion SIO_000772 23585512 NP673037.RASXOYLOywf6m7H99SSP4rdCd3N8WGVLNQ3MWvVRgS3R4130_provenance.
- NP673037.RASXOYLOywf6m7H99SSP4rdCd3N8WGVLNQ3MWvVRgS3R4130_assertion wasDerivedFrom befree-20150227 NP673037.RASXOYLOywf6m7H99SSP4rdCd3N8WGVLNQ3MWvVRgS3R4130_provenance.
- NP673037.RASXOYLOywf6m7H99SSP4rdCd3N8WGVLNQ3MWvVRgS3R4130_assertion wasGeneratedBy ECO_0000203 NP673037.RASXOYLOywf6m7H99SSP4rdCd3N8WGVLNQ3MWvVRgS3R4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP673037.RASXOYLOywf6m7H99SSP4rdCd3N8WGVLNQ3MWvVRgS3R4130_provenance.