Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1176873.RA7QaltO1rYe4CMMLrCM02CQ_km6141aMDS5OZHz0vt6o#provenance>. }
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- source_evidence_curated type ECO_0000205 provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." provenance.
- UNIPROT importedOn "2017-01-25" provenance.
- assertion wasGeneratedBy ECO_0000218 provenance.
- assertion wasDerivedFrom UNIPROT provenance.
- assertion SIO_000772 19191227 provenance.
- assertion evidence source_evidence_curated provenance.
- assertion description "[In addition, de novo LGI1 mutations are found in about 2% of sporadic cases with idiopathic partial epilepsy with auditory features, who are clinically similar to the majority of patients with ADLTE/ADPEAF but have no family history.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.