Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP3371.RAkvS4tTH95y7nFFrHNpB-WDBg7EEvhb0EHhlNspZ48RY130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP3371.RAkvS4tTH95y7nFFrHNpB-WDBg7EEvhb0EHhlNspZ48RY130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP3371.RAkvS4tTH95y7nFFrHNpB-WDBg7EEvhb0EHhlNspZ48RY130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP3371.RAkvS4tTH95y7nFFrHNpB-WDBg7EEvhb0EHhlNspZ48RY130_provenance.
- uniprot-20150221 importedOn "2015-02-21" NP3371.RAkvS4tTH95y7nFFrHNpB-WDBg7EEvhb0EHhlNspZ48RY130_provenance.
- NP3371.RAkvS4tTH95y7nFFrHNpB-WDBg7EEvhb0EHhlNspZ48RY130_assertion wasGeneratedBy ECO_0000218 NP3371.RAkvS4tTH95y7nFFrHNpB-WDBg7EEvhb0EHhlNspZ48RY130_provenance.
- NP3371.RAkvS4tTH95y7nFFrHNpB-WDBg7EEvhb0EHhlNspZ48RY130_assertion wasDerivedFrom uniprot-20150221 NP3371.RAkvS4tTH95y7nFFrHNpB-WDBg7EEvhb0EHhlNspZ48RY130_provenance.
- NP3371.RAkvS4tTH95y7nFFrHNpB-WDBg7EEvhb0EHhlNspZ48RY130_assertion SIO_000772 17136396 NP3371.RAkvS4tTH95y7nFFrHNpB-WDBg7EEvhb0EHhlNspZ48RY130_provenance.
- NP3371.RAkvS4tTH95y7nFFrHNpB-WDBg7EEvhb0EHhlNspZ48RY130_assertion evidence source_evidence_curated NP3371.RAkvS4tTH95y7nFFrHNpB-WDBg7EEvhb0EHhlNspZ48RY130_provenance.
- NP3371.RAkvS4tTH95y7nFFrHNpB-WDBg7EEvhb0EHhlNspZ48RY130_assertion description "[Functional analysis of a novel potassium channel (KCNA1) mutation in hereditary myokymia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3371.RAkvS4tTH95y7nFFrHNpB-WDBg7EEvhb0EHhlNspZ48RY130_provenance.