Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Bfc3691c082f0fcf1d858fcc68b1e3310> ?p ?o ?g. }
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- Bfc3691c082f0fcf1d858fcc68b1e3310 hasDbXref "https://orcid.org/0000-0001-8486-0558" @default.
- Bfc3691c082f0fcf1d858fcc68b1e3310 hasDbXref "https://www.epilepsydiagnosis.org/syndrome/benign-fam-nonfam-infantile-overview.html" @default.
- Bfc3691c082f0fcf1d858fcc68b1e3310 type Axiom @default.
- Bfc3691c082f0fcf1d858fcc68b1e3310 annotatedProperty IAO_0000115 @default.
- Bfc3691c082f0fcf1d858fcc68b1e3310 annotatedSource MONDO_0100024 @default.
- Bfc3691c082f0fcf1d858fcc68b1e3310 annotatedTarget "This syndrome is characterized by the onset of seizures between 3 and 20 months of age (peak 6 months). Seizures may be frequent at onset but usually remit within 1 year from the onset. In untreated cases there can be isolated or brief clusters of seizures within the period from onset to remission. A minority of individuals may have epilepsy in later life. Some patients (with PRRT2 mutations) may develop paroxysmal kinesiogenic dyskinesia in later life." @default.