Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP805067.RA6pjhnWZCxtIdg4NhxP8SoKIfYsCI_vAvmnmyFMmncgs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP805067.RA6pjhnWZCxtIdg4NhxP8SoKIfYsCI_vAvmnmyFMmncgs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP805067.RA6pjhnWZCxtIdg4NhxP8SoKIfYsCI_vAvmnmyFMmncgs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP805067.RA6pjhnWZCxtIdg4NhxP8SoKIfYsCI_vAvmnmyFMmncgs130_provenance.
- NP805067.RA6pjhnWZCxtIdg4NhxP8SoKIfYsCI_vAvmnmyFMmncgs130_assertion description "[GSS and PrP-CAA are associated with point mutations of the prion protein gene (PRNP); these conditions show a broad spectrum of clinical presentation, the main signs being ataxia, spastic paraparesis, extrapyramidal signs and dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP805067.RA6pjhnWZCxtIdg4NhxP8SoKIfYsCI_vAvmnmyFMmncgs130_provenance.
- NP805067.RA6pjhnWZCxtIdg4NhxP8SoKIfYsCI_vAvmnmyFMmncgs130_assertion evidence source_evidence_literature NP805067.RA6pjhnWZCxtIdg4NhxP8SoKIfYsCI_vAvmnmyFMmncgs130_provenance.
- NP805067.RA6pjhnWZCxtIdg4NhxP8SoKIfYsCI_vAvmnmyFMmncgs130_assertion SIO_000772 8737929 NP805067.RA6pjhnWZCxtIdg4NhxP8SoKIfYsCI_vAvmnmyFMmncgs130_provenance.
- NP805067.RA6pjhnWZCxtIdg4NhxP8SoKIfYsCI_vAvmnmyFMmncgs130_assertion wasDerivedFrom befree-20140225 NP805067.RA6pjhnWZCxtIdg4NhxP8SoKIfYsCI_vAvmnmyFMmncgs130_provenance.
- NP805067.RA6pjhnWZCxtIdg4NhxP8SoKIfYsCI_vAvmnmyFMmncgs130_assertion wasGeneratedBy ECO_0000203 NP805067.RA6pjhnWZCxtIdg4NhxP8SoKIfYsCI_vAvmnmyFMmncgs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP805067.RA6pjhnWZCxtIdg4NhxP8SoKIfYsCI_vAvmnmyFMmncgs130_provenance.