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- Beecb0b8e6a3d44417948f0c0de6f09f4 NCIT_P378 "NCI" @default.
- Beecb0b8e6a3d44417948f0c0de6f09f4 type Axiom @default.
- Beecb0b8e6a3d44417948f0c0de6f09f4 annotatedProperty IAO_0000115 @default.
- Beecb0b8e6a3d44417948f0c0de6f09f4 annotatedSource NCIT_C75488 @default.
- Beecb0b8e6a3d44417948f0c0de6f09f4 annotatedTarget "A progressive neurologic disorder caused by mutations in the MECP2 gene on chromosome X. It almost exclusively affects girls. It is characterized by language and learning difficulties, poor communication skills, and repetitive hand motions. Other signs and symptoms include microcephaly, scoliosis, breathing abnormalities, and sleep disturbances." @default.