Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP815.RAiSW3ESlPnZu7u5I6W1NcjPFoSISrf7Vr3OdOUqZff8c130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP815.RAiSW3ESlPnZu7u5I6W1NcjPFoSISrf7Vr3OdOUqZff8c130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP815.RAiSW3ESlPnZu7u5I6W1NcjPFoSISrf7Vr3OdOUqZff8c130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP815.RAiSW3ESlPnZu7u5I6W1NcjPFoSISrf7Vr3OdOUqZff8c130_provenance.
- uniprot-20150221 importedOn "2015-02-21" NP815.RAiSW3ESlPnZu7u5I6W1NcjPFoSISrf7Vr3OdOUqZff8c130_provenance.
- NP815.RAiSW3ESlPnZu7u5I6W1NcjPFoSISrf7Vr3OdOUqZff8c130_assertion wasGeneratedBy ECO_0000218 NP815.RAiSW3ESlPnZu7u5I6W1NcjPFoSISrf7Vr3OdOUqZff8c130_provenance.
- NP815.RAiSW3ESlPnZu7u5I6W1NcjPFoSISrf7Vr3OdOUqZff8c130_assertion wasDerivedFrom uniprot-20150221 NP815.RAiSW3ESlPnZu7u5I6W1NcjPFoSISrf7Vr3OdOUqZff8c130_provenance.
- NP815.RAiSW3ESlPnZu7u5I6W1NcjPFoSISrf7Vr3OdOUqZff8c130_assertion SIO_000772 21035104 NP815.RAiSW3ESlPnZu7u5I6W1NcjPFoSISrf7Vr3OdOUqZff8c130_provenance.
- NP815.RAiSW3ESlPnZu7u5I6W1NcjPFoSISrf7Vr3OdOUqZff8c130_assertion evidence source_evidence_curated NP815.RAiSW3ESlPnZu7u5I6W1NcjPFoSISrf7Vr3OdOUqZff8c130_provenance.
- NP815.RAiSW3ESlPnZu7u5I6W1NcjPFoSISrf7Vr3OdOUqZff8c130_assertion description "[PDYN mutations are identified in a small subset of ataxia families, indicating that SCA23 is an infrequent SCA type (a1/40.5%) in the Netherlands and suggesting further genetic SCA heterogeneity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP815.RAiSW3ESlPnZu7u5I6W1NcjPFoSISrf7Vr3OdOUqZff8c130_provenance.