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- Bb08afc307ba764ec6421d19c32fbd263 NCIT_P378 "NCI" @default.
- Bb08afc307ba764ec6421d19c32fbd263 type Axiom @default.
- Bb08afc307ba764ec6421d19c32fbd263 annotatedProperty IAO_0000115 @default.
- Bb08afc307ba764ec6421d19c32fbd263 annotatedSource NCIT_C177545 @default.
- Bb08afc307ba764ec6421d19c32fbd263 annotatedTarget "An autosomal dominant condition caused by mutation(s) in the GRIN2D gene, encoding glutamate receptor ionotropic, NMDA 2D. It is characterized by developmental delay and intractable seizures." @default.