Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP286.RA8HRVku-gESK2tQZsKPIsA6OpN-jNifsuvC8fMbMh388130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP286.RA8HRVku-gESK2tQZsKPIsA6OpN-jNifsuvC8fMbMh388130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP286.RA8HRVku-gESK2tQZsKPIsA6OpN-jNifsuvC8fMbMh388130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP286.RA8HRVku-gESK2tQZsKPIsA6OpN-jNifsuvC8fMbMh388130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP286.RA8HRVku-gESK2tQZsKPIsA6OpN-jNifsuvC8fMbMh388130_provenance.
- NP286.RA8HRVku-gESK2tQZsKPIsA6OpN-jNifsuvC8fMbMh388130_assertion wasGeneratedBy ECO_0000218 NP286.RA8HRVku-gESK2tQZsKPIsA6OpN-jNifsuvC8fMbMh388130_provenance.
- NP286.RA8HRVku-gESK2tQZsKPIsA6OpN-jNifsuvC8fMbMh388130_assertion wasDerivedFrom uniprot-2016 NP286.RA8HRVku-gESK2tQZsKPIsA6OpN-jNifsuvC8fMbMh388130_provenance.
- NP286.RA8HRVku-gESK2tQZsKPIsA6OpN-jNifsuvC8fMbMh388130_assertion SIO_000772 10412802 NP286.RA8HRVku-gESK2tQZsKPIsA6OpN-jNifsuvC8fMbMh388130_provenance.
- NP286.RA8HRVku-gESK2tQZsKPIsA6OpN-jNifsuvC8fMbMh388130_assertion evidence source_evidence_curated NP286.RA8HRVku-gESK2tQZsKPIsA6OpN-jNifsuvC8fMbMh388130_provenance.
- NP286.RA8HRVku-gESK2tQZsKPIsA6OpN-jNifsuvC8fMbMh388130_assertion description "[Recently intronic and exonic mutations in the Tau gene have been found to be associated with familial neurodegenerative syndromes characterized not only by a predominantly frontotemporal dementia but also by the presence of neurological signs consistent with the dysfunction of multiple subcortical neuronal circuitries.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP286.RA8HRVku-gESK2tQZsKPIsA6OpN-jNifsuvC8fMbMh388130_provenance.