Matches in Nanopublications for { ?s ?p "[Severe myoclonic epilepsy of infancy (SMEI) or Dravet syndrome (DS) is a distinctive epilepsy syndrome often associated with de novo mutations in the SCN1A gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[Severe myoclonic epilepsy of infancy (SMEI) or Dravet syndrome (DS) is a distinctive epilepsy syndrome often associated with de novo mutations in the SCN1A gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP761549.RAlSig20Z8rqoGLXSMDdKVFWRJ0ZEaJS5qOljY43uml-Y130_assertion description "[Severe myoclonic epilepsy of infancy (SMEI) or Dravet syndrome (DS) is a distinctive epilepsy syndrome often associated with de novo mutations in the SCN1A gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP761549.RAlSig20Z8rqoGLXSMDdKVFWRJ0ZEaJS5qOljY43uml-Y130_provenance.