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- B661af3ba9f4d85d96e3d39e7eba57dc1 hasDbXref "PMID:28276062" @default.
- B661af3ba9f4d85d96e3d39e7eba57dc1 hasDbXref "https://orcid.org/0000-0001-8486-0558" @default.
- B661af3ba9f4d85d96e3d39e7eba57dc1 hasDbXref "https://www.epilepsydiagnosis.org/syndrome/self-limited-neonatal-overview.html" @default.
- B661af3ba9f4d85d96e3d39e7eba57dc1 type Axiom @default.
- B661af3ba9f4d85d96e3d39e7eba57dc1 annotatedProperty IAO_0000115 @default.
- B661af3ba9f4d85d96e3d39e7eba57dc1 annotatedSource MONDO_0100023 @default.
- B661af3ba9f4d85d96e3d39e7eba57dc1 annotatedTarget "A neonatal/infantile epilepsy syndrome that is characterized by the onset of seizures that start in the in the neonate between day 1 and 7 of life and are often unilateral clonic events that recur and may alternate sides from seizure to seizure. Seizures can be repetitive over hours to days. Seizures remit by 4-6 months of age. A proportion of those affected may have seizures in later life. The child is expected to have typical developmental progress." @default.