Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP806350.RAfnA2PzYwdW1NwvoOppMGceLUM0Kc-FlLo1osqYb-BDY130_assertion> ?p ?o ?g. }
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- NP806350.RAfnA2PzYwdW1NwvoOppMGceLUM0Kc-FlLo1osqYb-BDY130_assertion type Assertion NP806350.RAfnA2PzYwdW1NwvoOppMGceLUM0Kc-FlLo1osqYb-BDY130_head.
- NP806350.RAfnA2PzYwdW1NwvoOppMGceLUM0Kc-FlLo1osqYb-BDY130_assertion description "[Here we describe identification of the causative gene in autosomal-dominant partial epilepsy with auditory features (ADPEAF, MIM 600512), a rare form of idiopathic lateral temporal lobe epilepsy characterized by partial seizures with auditory disturbances.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP806350.RAfnA2PzYwdW1NwvoOppMGceLUM0Kc-FlLo1osqYb-BDY130_provenance.
- NP806350.RAfnA2PzYwdW1NwvoOppMGceLUM0Kc-FlLo1osqYb-BDY130_assertion evidence source_evidence_literature NP806350.RAfnA2PzYwdW1NwvoOppMGceLUM0Kc-FlLo1osqYb-BDY130_provenance.
- NP806350.RAfnA2PzYwdW1NwvoOppMGceLUM0Kc-FlLo1osqYb-BDY130_assertion SIO_000772 11810107 NP806350.RAfnA2PzYwdW1NwvoOppMGceLUM0Kc-FlLo1osqYb-BDY130_provenance.
- NP806350.RAfnA2PzYwdW1NwvoOppMGceLUM0Kc-FlLo1osqYb-BDY130_assertion wasDerivedFrom befree-20140225 NP806350.RAfnA2PzYwdW1NwvoOppMGceLUM0Kc-FlLo1osqYb-BDY130_provenance.
- NP806350.RAfnA2PzYwdW1NwvoOppMGceLUM0Kc-FlLo1osqYb-BDY130_assertion wasGeneratedBy ECO_0000203 NP806350.RAfnA2PzYwdW1NwvoOppMGceLUM0Kc-FlLo1osqYb-BDY130_provenance.