Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP293983.RASESUmcsbEUAOnCSpv0Y6wMiQHaaD965MssgdaTQoDJI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP293983.RASESUmcsbEUAOnCSpv0Y6wMiQHaaD965MssgdaTQoDJI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP293983.RASESUmcsbEUAOnCSpv0Y6wMiQHaaD965MssgdaTQoDJI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP293983.RASESUmcsbEUAOnCSpv0Y6wMiQHaaD965MssgdaTQoDJI130_provenance.
- NP293983.RASESUmcsbEUAOnCSpv0Y6wMiQHaaD965MssgdaTQoDJI130_assertion description "[We hypothesized that mutations in SCARB2 might account for unsolved cases of progressive myoclonus epilepsy (PME) without renal impairment, especially those resembling Unverricht-Lundborg disease (ULD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP293983.RASESUmcsbEUAOnCSpv0Y6wMiQHaaD965MssgdaTQoDJI130_provenance.
- NP293983.RASESUmcsbEUAOnCSpv0Y6wMiQHaaD965MssgdaTQoDJI130_assertion evidence source_evidence_literature NP293983.RASESUmcsbEUAOnCSpv0Y6wMiQHaaD965MssgdaTQoDJI130_provenance.
- NP293983.RASESUmcsbEUAOnCSpv0Y6wMiQHaaD965MssgdaTQoDJI130_assertion SIO_000772 19847901 NP293983.RASESUmcsbEUAOnCSpv0Y6wMiQHaaD965MssgdaTQoDJI130_provenance.
- NP293983.RASESUmcsbEUAOnCSpv0Y6wMiQHaaD965MssgdaTQoDJI130_assertion wasDerivedFrom befree-20150227 NP293983.RASESUmcsbEUAOnCSpv0Y6wMiQHaaD965MssgdaTQoDJI130_provenance.
- NP293983.RASESUmcsbEUAOnCSpv0Y6wMiQHaaD965MssgdaTQoDJI130_assertion wasGeneratedBy ECO_0000203 NP293983.RASESUmcsbEUAOnCSpv0Y6wMiQHaaD965MssgdaTQoDJI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP293983.RASESUmcsbEUAOnCSpv0Y6wMiQHaaD965MssgdaTQoDJI130_provenance.