Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP7621.RAknYfRleHBYKiEyJvOCke49-QiPyhHuZZsr9Ues63Y1Q130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP7621.RAknYfRleHBYKiEyJvOCke49-QiPyhHuZZsr9Ues63Y1Q130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP7621.RAknYfRleHBYKiEyJvOCke49-QiPyhHuZZsr9Ues63Y1Q130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP7621.RAknYfRleHBYKiEyJvOCke49-QiPyhHuZZsr9Ues63Y1Q130_provenance.
- NP7621.RAknYfRleHBYKiEyJvOCke49-QiPyhHuZZsr9Ues63Y1Q130_assertion description "[GRIN2A mutations in acquired epileptic aphasia and related childhood focal epilepsies and encephalopathies with speech and language dysfunction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP7621.RAknYfRleHBYKiEyJvOCke49-QiPyhHuZZsr9Ues63Y1Q130_provenance.
- NP7621.RAknYfRleHBYKiEyJvOCke49-QiPyhHuZZsr9Ues63Y1Q130_assertion evidence source_evidence_curated NP7621.RAknYfRleHBYKiEyJvOCke49-QiPyhHuZZsr9Ues63Y1Q130_provenance.
- NP7621.RAknYfRleHBYKiEyJvOCke49-QiPyhHuZZsr9Ues63Y1Q130_assertion SIO_000772 23933820 NP7621.RAknYfRleHBYKiEyJvOCke49-QiPyhHuZZsr9Ues63Y1Q130_provenance.
- NP7621.RAknYfRleHBYKiEyJvOCke49-QiPyhHuZZsr9Ues63Y1Q130_assertion wasDerivedFrom uniprot-2016 NP7621.RAknYfRleHBYKiEyJvOCke49-QiPyhHuZZsr9Ues63Y1Q130_provenance.
- NP7621.RAknYfRleHBYKiEyJvOCke49-QiPyhHuZZsr9Ues63Y1Q130_assertion wasGeneratedBy ECO_0000218 NP7621.RAknYfRleHBYKiEyJvOCke49-QiPyhHuZZsr9Ues63Y1Q130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP7621.RAknYfRleHBYKiEyJvOCke49-QiPyhHuZZsr9Ues63Y1Q130_provenance.