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- B82e9f651a79a7579d25a07ae9d1aa25b NCIT_P378 "NCI" @default.
- B82e9f651a79a7579d25a07ae9d1aa25b type Axiom @default.
- B82e9f651a79a7579d25a07ae9d1aa25b annotatedProperty IAO_0000115 @default.
- B82e9f651a79a7579d25a07ae9d1aa25b annotatedSource NCIT_C177545 @default.
- B82e9f651a79a7579d25a07ae9d1aa25b 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.