Matches in Nanopublications for { ?s ?p "[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."@en ?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 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 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.
- NP1249534.RAvmmKL-E5qqeMJM5RkdS02hpjujkFwKAsQzsDcTopRxQ130_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." NP1249534.RAvmmKL-E5qqeMJM5RkdS02hpjujkFwKAsQzsDcTopRxQ130_provenance.
- NP1249527.RA-SQsIDoSToyke-7Fn9KuVR7cEcj_Rr5q862UAd4tzjo130_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." NP1249527.RA-SQsIDoSToyke-7Fn9KuVR7cEcj_Rr5q862UAd4tzjo130_provenance.