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- B68dec1c87b5b591389d66e00c0a2ec06 NCIT_P378 "NCI" @default.
- B68dec1c87b5b591389d66e00c0a2ec06 type Axiom @default.
- B68dec1c87b5b591389d66e00c0a2ec06 annotatedProperty IAO_0000115 @default.
- B68dec1c87b5b591389d66e00c0a2ec06 annotatedSource NCIT_C177544 @default.
- B68dec1c87b5b591389d66e00c0a2ec06 annotatedTarget "An X-linked genetic condition caused by duplication of a small segment of Xq25, which may encompass the GRIA3 and STAG2 genes, encoding glutamate receptor 3 and cohesin subunit SA-2. It is characterized by intellectual disability and distinctive facial dysmorphisms." @default.