Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP946546.RAIRqkIxa0418GTD8P_IMRzOi7LxGnQhAWmKHth7XsnhY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP946546.RAIRqkIxa0418GTD8P_IMRzOi7LxGnQhAWmKHth7XsnhY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP946546.RAIRqkIxa0418GTD8P_IMRzOi7LxGnQhAWmKHth7XsnhY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP946546.RAIRqkIxa0418GTD8P_IMRzOi7LxGnQhAWmKHth7XsnhY130_provenance.
- NP946546.RAIRqkIxa0418GTD8P_IMRzOi7LxGnQhAWmKHth7XsnhY130_assertion description "[Although the role of 14-3-3 proteins in the pathogenesis of prion diseases remains unknown, the detection of altered levels of isoforms of the 14-3-3 protein in the cerebrospinal fluid is considered a biomarker for diagnosis of sporadic Creutzfeldt-Jakob disease (sCJD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP946546.RAIRqkIxa0418GTD8P_IMRzOi7LxGnQhAWmKHth7XsnhY130_provenance.
- NP946546.RAIRqkIxa0418GTD8P_IMRzOi7LxGnQhAWmKHth7XsnhY130_assertion evidence source_evidence_literature NP946546.RAIRqkIxa0418GTD8P_IMRzOi7LxGnQhAWmKHth7XsnhY130_provenance.
- NP946546.RAIRqkIxa0418GTD8P_IMRzOi7LxGnQhAWmKHth7XsnhY130_assertion SIO_000772 21739144 NP946546.RAIRqkIxa0418GTD8P_IMRzOi7LxGnQhAWmKHth7XsnhY130_provenance.
- NP946546.RAIRqkIxa0418GTD8P_IMRzOi7LxGnQhAWmKHth7XsnhY130_assertion wasDerivedFrom befree-20150227 NP946546.RAIRqkIxa0418GTD8P_IMRzOi7LxGnQhAWmKHth7XsnhY130_provenance.
- NP946546.RAIRqkIxa0418GTD8P_IMRzOi7LxGnQhAWmKHth7XsnhY130_assertion wasGeneratedBy ECO_0000203 NP946546.RAIRqkIxa0418GTD8P_IMRzOi7LxGnQhAWmKHth7XsnhY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP946546.RAIRqkIxa0418GTD8P_IMRzOi7LxGnQhAWmKHth7XsnhY130_provenance.