Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP856375.RABGU57IgsLTgHsANUsvNfQUQ35SFt5NwmsjEZnNmZWkQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP856375.RABGU57IgsLTgHsANUsvNfQUQ35SFt5NwmsjEZnNmZWkQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP856375.RABGU57IgsLTgHsANUsvNfQUQ35SFt5NwmsjEZnNmZWkQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP856375.RABGU57IgsLTgHsANUsvNfQUQ35SFt5NwmsjEZnNmZWkQ130_provenance.
- NP856375.RABGU57IgsLTgHsANUsvNfQUQ35SFt5NwmsjEZnNmZWkQ130_assertion description "[GSS is defined as a neurodegenerative disease `in family with dominantly inherited progressive ataxia and/or dementia): encephalo(myelo)pathy with multi-centric PrP plaques`.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP856375.RABGU57IgsLTgHsANUsvNfQUQ35SFt5NwmsjEZnNmZWkQ130_provenance.
- NP856375.RABGU57IgsLTgHsANUsvNfQUQ35SFt5NwmsjEZnNmZWkQ130_assertion evidence source_evidence_literature NP856375.RABGU57IgsLTgHsANUsvNfQUQ35SFt5NwmsjEZnNmZWkQ130_provenance.
- NP856375.RABGU57IgsLTgHsANUsvNfQUQ35SFt5NwmsjEZnNmZWkQ130_assertion SIO_000772 16903147 NP856375.RABGU57IgsLTgHsANUsvNfQUQ35SFt5NwmsjEZnNmZWkQ130_provenance.
- NP856375.RABGU57IgsLTgHsANUsvNfQUQ35SFt5NwmsjEZnNmZWkQ130_assertion wasDerivedFrom befree-20140225 NP856375.RABGU57IgsLTgHsANUsvNfQUQ35SFt5NwmsjEZnNmZWkQ130_provenance.
- NP856375.RABGU57IgsLTgHsANUsvNfQUQ35SFt5NwmsjEZnNmZWkQ130_assertion wasGeneratedBy ECO_0000203 NP856375.RABGU57IgsLTgHsANUsvNfQUQ35SFt5NwmsjEZnNmZWkQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP856375.RABGU57IgsLTgHsANUsvNfQUQ35SFt5NwmsjEZnNmZWkQ130_provenance.