Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP378.RA9qS2XwGbHQWHgWFvxJvb56gbKI67p5jGYsRbrFs9z5g130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP378.RA9qS2XwGbHQWHgWFvxJvb56gbKI67p5jGYsRbrFs9z5g130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP378.RA9qS2XwGbHQWHgWFvxJvb56gbKI67p5jGYsRbrFs9z5g130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP378.RA9qS2XwGbHQWHgWFvxJvb56gbKI67p5jGYsRbrFs9z5g130_provenance.
- NP378.RA9qS2XwGbHQWHgWFvxJvb56gbKI67p5jGYsRbrFs9z5g130_assertion description "[Familial cortical myoclonus with a mutation in NOL3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP378.RA9qS2XwGbHQWHgWFvxJvb56gbKI67p5jGYsRbrFs9z5g130_provenance.
- NP378.RA9qS2XwGbHQWHgWFvxJvb56gbKI67p5jGYsRbrFs9z5g130_assertion evidence source_evidence_curated NP378.RA9qS2XwGbHQWHgWFvxJvb56gbKI67p5jGYsRbrFs9z5g130_provenance.
- NP378.RA9qS2XwGbHQWHgWFvxJvb56gbKI67p5jGYsRbrFs9z5g130_assertion SIO_000772 22926851 NP378.RA9qS2XwGbHQWHgWFvxJvb56gbKI67p5jGYsRbrFs9z5g130_provenance.
- NP378.RA9qS2XwGbHQWHgWFvxJvb56gbKI67p5jGYsRbrFs9z5g130_assertion wasDerivedFrom uniprot-20150221 NP378.RA9qS2XwGbHQWHgWFvxJvb56gbKI67p5jGYsRbrFs9z5g130_provenance.
- NP378.RA9qS2XwGbHQWHgWFvxJvb56gbKI67p5jGYsRbrFs9z5g130_assertion wasGeneratedBy ECO_0000218 NP378.RA9qS2XwGbHQWHgWFvxJvb56gbKI67p5jGYsRbrFs9z5g130_provenance.
- uniprot-20150221 importedOn "2015-02-21" NP378.RA9qS2XwGbHQWHgWFvxJvb56gbKI67p5jGYsRbrFs9z5g130_provenance.