Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP727025.RAX0J-9vmiMJnr0BgNTX3hFXO88ee4YS2oidRsGBhawPg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP727025.RAX0J-9vmiMJnr0BgNTX3hFXO88ee4YS2oidRsGBhawPg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP727025.RAX0J-9vmiMJnr0BgNTX3hFXO88ee4YS2oidRsGBhawPg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP727025.RAX0J-9vmiMJnr0BgNTX3hFXO88ee4YS2oidRsGBhawPg130_provenance.
- NP727025.RAX0J-9vmiMJnr0BgNTX3hFXO88ee4YS2oidRsGBhawPg130_assertion description "[Furthermore, the linkage of mutations within the PRNP gene with phenotypic appearance of Creutzfeldt-Jakob disease and Gerstmann-Str�ussler-Scheinker syndrome points to importance of the PrP gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP727025.RAX0J-9vmiMJnr0BgNTX3hFXO88ee4YS2oidRsGBhawPg130_provenance.
- NP727025.RAX0J-9vmiMJnr0BgNTX3hFXO88ee4YS2oidRsGBhawPg130_assertion evidence source_evidence_literature NP727025.RAX0J-9vmiMJnr0BgNTX3hFXO88ee4YS2oidRsGBhawPg130_provenance.
- NP727025.RAX0J-9vmiMJnr0BgNTX3hFXO88ee4YS2oidRsGBhawPg130_assertion SIO_000772 7922109 NP727025.RAX0J-9vmiMJnr0BgNTX3hFXO88ee4YS2oidRsGBhawPg130_provenance.
- NP727025.RAX0J-9vmiMJnr0BgNTX3hFXO88ee4YS2oidRsGBhawPg130_assertion wasDerivedFrom befree-20150227 NP727025.RAX0J-9vmiMJnr0BgNTX3hFXO88ee4YS2oidRsGBhawPg130_provenance.
- NP727025.RAX0J-9vmiMJnr0BgNTX3hFXO88ee4YS2oidRsGBhawPg130_assertion wasGeneratedBy ECO_0000203 NP727025.RAX0J-9vmiMJnr0BgNTX3hFXO88ee4YS2oidRsGBhawPg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP727025.RAX0J-9vmiMJnr0BgNTX3hFXO88ee4YS2oidRsGBhawPg130_provenance.