Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP308558.RABSoIhU2vmXLxAgPxrMgzUFzWb3fvXtDIeWVCgAK2IuU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP308558.RABSoIhU2vmXLxAgPxrMgzUFzWb3fvXtDIeWVCgAK2IuU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP308558.RABSoIhU2vmXLxAgPxrMgzUFzWb3fvXtDIeWVCgAK2IuU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP308558.RABSoIhU2vmXLxAgPxrMgzUFzWb3fvXtDIeWVCgAK2IuU130_provenance.
- NP308558.RABSoIhU2vmXLxAgPxrMgzUFzWb3fvXtDIeWVCgAK2IuU130_assertion description "[However, since specific polymorphisms and mutations in the tau gene lead to diverse phenotypes, it is plausible that additional genetic or epigenetic factors influence the clinical and pathological manifestations of both familial and sporadic tauopathies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP308558.RABSoIhU2vmXLxAgPxrMgzUFzWb3fvXtDIeWVCgAK2IuU130_provenance.
- NP308558.RABSoIhU2vmXLxAgPxrMgzUFzWb3fvXtDIeWVCgAK2IuU130_assertion evidence source_evidence_literature NP308558.RABSoIhU2vmXLxAgPxrMgzUFzWb3fvXtDIeWVCgAK2IuU130_provenance.
- NP308558.RABSoIhU2vmXLxAgPxrMgzUFzWb3fvXtDIeWVCgAK2IuU130_assertion SIO_000772 11207421 NP308558.RABSoIhU2vmXLxAgPxrMgzUFzWb3fvXtDIeWVCgAK2IuU130_provenance.
- NP308558.RABSoIhU2vmXLxAgPxrMgzUFzWb3fvXtDIeWVCgAK2IuU130_assertion wasDerivedFrom befree-2016 NP308558.RABSoIhU2vmXLxAgPxrMgzUFzWb3fvXtDIeWVCgAK2IuU130_provenance.
- NP308558.RABSoIhU2vmXLxAgPxrMgzUFzWb3fvXtDIeWVCgAK2IuU130_assertion wasGeneratedBy ECO_0000203 NP308558.RABSoIhU2vmXLxAgPxrMgzUFzWb3fvXtDIeWVCgAK2IuU130_provenance.
- befree-2016 importedOn "2016-02-19" NP308558.RABSoIhU2vmXLxAgPxrMgzUFzWb3fvXtDIeWVCgAK2IuU130_provenance.