Matches in Nanopublications for { ?s ?p "[Epilepsy phenotype associated with a chromosome 2q24.3 deletion involving SCN1A: Migrating partial seizures of infancy or atypical Dravet syndrome?]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[Epilepsy phenotype associated with a chromosome 2q24.3 deletion involving SCN1A: Migrating partial seizures of infancy or atypical Dravet syndrome?]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1249535.RAs0rmC6WIvnzvemIci_DHOPfyn1K3YEdOpCsfdANi59c130_assertion description "[Epilepsy phenotype associated with a chromosome 2q24.3 deletion involving SCN1A: Migrating partial seizures of infancy or atypical Dravet syndrome?]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1249535.RAs0rmC6WIvnzvemIci_DHOPfyn1K3YEdOpCsfdANi59c130_provenance.
- NP1249529.RALnMj7CEp6vHIFMI60tGq3MLjD6KBuYw-0zrE6GWUMiA130_assertion description "[Epilepsy phenotype associated with a chromosome 2q24.3 deletion involving SCN1A: Migrating partial seizures of infancy or atypical Dravet syndrome?]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1249529.RALnMj7CEp6vHIFMI60tGq3MLjD6KBuYw-0zrE6GWUMiA130_provenance.
- NP1249537.RA8-MT-yXWV9ee7OCWQrtafkGLdGSPZHtueD4s7SgeZkY130_assertion description "[Epilepsy phenotype associated with a chromosome 2q24.3 deletion involving SCN1A: Migrating partial seizures of infancy or atypical Dravet syndrome?]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1249537.RA8-MT-yXWV9ee7OCWQrtafkGLdGSPZHtueD4s7SgeZkY130_provenance.