Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP926730.RAPjaRv3_1pNbMAS0HD_xPHYkX50REKT9_d9S4sjpEqJ4#assertion> ?p ?o ?g. }
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- assertion description "[Two cases with partial deletion of SCN1A and SCN9A and whole SCN1A deletion had an epilepsy phenotype of Dravet syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion evidence source_evidence_literature provenance.
- assertion SIO_000772 25524840 provenance.
- assertion wasDerivedFrom BEFREE provenance.
- assertion wasGeneratedBy ECO_0000203 provenance.