Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP3765.RAFjDqOUlLJl0MYTJtcD50X1ZK44JHh318oAfwCMcJWr8130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP3765.RAFjDqOUlLJl0MYTJtcD50X1ZK44JHh318oAfwCMcJWr8130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP3765.RAFjDqOUlLJl0MYTJtcD50X1ZK44JHh318oAfwCMcJWr8130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP3765.RAFjDqOUlLJl0MYTJtcD50X1ZK44JHh318oAfwCMcJWr8130_provenance.
- NP3765.RAFjDqOUlLJl0MYTJtcD50X1ZK44JHh318oAfwCMcJWr8130_assertion wasGeneratedBy ECO_0000218 NP3765.RAFjDqOUlLJl0MYTJtcD50X1ZK44JHh318oAfwCMcJWr8130_provenance.
- NP3765.RAFjDqOUlLJl0MYTJtcD50X1ZK44JHh318oAfwCMcJWr8130_assertion wasDerivedFrom uniprot-20130724 NP3765.RAFjDqOUlLJl0MYTJtcD50X1ZK44JHh318oAfwCMcJWr8130_provenance.
- NP3765.RAFjDqOUlLJl0MYTJtcD50X1ZK44JHh318oAfwCMcJWr8130_assertion SIO_000772 12771268 NP3765.RAFjDqOUlLJl0MYTJtcD50X1ZK44JHh318oAfwCMcJWr8130_provenance.
- NP3765.RAFjDqOUlLJl0MYTJtcD50X1ZK44JHh318oAfwCMcJWr8130_assertion evidence source_evidence_curated NP3765.RAFjDqOUlLJl0MYTJtcD50X1ZK44JHh318oAfwCMcJWr8130_provenance.
- NP3765.RAFjDqOUlLJl0MYTJtcD50X1ZK44JHh318oAfwCMcJWr8130_assertion description "[Autosomal dominant partial epilepsy with auditory features (ADPEAF) is a rare idiopathic epilepsy syndrome caused by mutations in the leucine-rich, glioma-inactivated 1 (LGI1) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3765.RAFjDqOUlLJl0MYTJtcD50X1ZK44JHh318oAfwCMcJWr8130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP3765.RAFjDqOUlLJl0MYTJtcD50X1ZK44JHh318oAfwCMcJWr8130_provenance.