Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1246857.RAfM1wwmB8CSY_RkLrIk-35lG0lzg0xZU8ppOU138YXEY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1246857.RAfM1wwmB8CSY_RkLrIk-35lG0lzg0xZU8ppOU138YXEY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1246857.RAfM1wwmB8CSY_RkLrIk-35lG0lzg0xZU8ppOU138YXEY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1246857.RAfM1wwmB8CSY_RkLrIk-35lG0lzg0xZU8ppOU138YXEY130_provenance.
- NP1246857.RAfM1wwmB8CSY_RkLrIk-35lG0lzg0xZU8ppOU138YXEY130_assertion description "[Creutzfeldt-Jakob disease associated with a V203I homozygous mutation in the prion protein gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1246857.RAfM1wwmB8CSY_RkLrIk-35lG0lzg0xZU8ppOU138YXEY130_provenance.
- NP1246857.RAfM1wwmB8CSY_RkLrIk-35lG0lzg0xZU8ppOU138YXEY130_assertion evidence source_evidence_literature NP1246857.RAfM1wwmB8CSY_RkLrIk-35lG0lzg0xZU8ppOU138YXEY130_provenance.
- NP1246857.RAfM1wwmB8CSY_RkLrIk-35lG0lzg0xZU8ppOU138YXEY130_assertion SIO_000772 25495585 NP1246857.RAfM1wwmB8CSY_RkLrIk-35lG0lzg0xZU8ppOU138YXEY130_provenance.
- NP1246857.RAfM1wwmB8CSY_RkLrIk-35lG0lzg0xZU8ppOU138YXEY130_assertion wasDerivedFrom befree-2016 NP1246857.RAfM1wwmB8CSY_RkLrIk-35lG0lzg0xZU8ppOU138YXEY130_provenance.
- NP1246857.RAfM1wwmB8CSY_RkLrIk-35lG0lzg0xZU8ppOU138YXEY130_assertion wasGeneratedBy ECO_0000203 NP1246857.RAfM1wwmB8CSY_RkLrIk-35lG0lzg0xZU8ppOU138YXEY130_provenance.
- befree-2016 importedOn "2016-02-19" NP1246857.RAfM1wwmB8CSY_RkLrIk-35lG0lzg0xZU8ppOU138YXEY130_provenance.