Matches in Nanopublications for { ?s ?p "[Most mutations in SCN1A-related epilepsies are novel and when an infant presents with febrile seizures (FS) it is uncertain if they will have simple FS, FS+, or develop a severe epilepsy such as Dravet syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP866374.RAD1ZO-YddUHwrY76HMVDTRjls0qNoDq9RswHsV749wW8130_assertion description "[Most mutations in SCN1A-related epilepsies are novel and when an infant presents with febrile seizures (FS) it is uncertain if they will have simple FS, FS+, or develop a severe epilepsy such as Dravet syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP866374.RAD1ZO-YddUHwrY76HMVDTRjls0qNoDq9RswHsV749wW8130_provenance.
- NP6495.RAUnszF42u5BKYaYS3G6OSI0elZo0xam-GnarOpaKEsgQ130_assertion description "[Most mutations in SCN1A-related epilepsies are novel and when an infant presents with febrile seizures (FS) it is uncertain if they will have simple FS, FS+, or develop a severe epilepsy such as Dravet syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP6495.RAUnszF42u5BKYaYS3G6OSI0elZo0xam-GnarOpaKEsgQ130_provenance.
- assertion description "[Most mutations in SCN1A-related epilepsies are novel and when an infant presents with febrile seizures (FS) it is uncertain if they will have simple FS, FS+, or develop a severe epilepsy such as Dravet syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Most mutations in SCN1A-related epilepsies are novel and when an infant presents with febrile seizures (FS) it is uncertain if they will have simple FS, FS+, or develop a severe epilepsy such as Dravet syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Most mutations in SCN1A-related epilepsies are novel and when an infant presents with febrile seizures (FS) it is uncertain if they will have simple FS, FS+, or develop a severe epilepsy such as Dravet syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP866373.RANEe_5N88drrU_Z8Y6QwohwdCE8MFVQmiHUJB1yGH-D0130_assertion description "[Most mutations in SCN1A-related epilepsies are novel and when an infant presents with febrile seizures (FS) it is uncertain if they will have simple FS, FS+, or develop a severe epilepsy such as Dravet syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP866373.RANEe_5N88drrU_Z8Y6QwohwdCE8MFVQmiHUJB1yGH-D0130_provenance.