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- B037b4d3470574f6f4c99efe88a069079 NCIT_P378 "NCI" @default.
- B037b4d3470574f6f4c99efe88a069079 type Axiom @default.
- B037b4d3470574f6f4c99efe88a069079 annotatedProperty IAO_0000115 @default.
- B037b4d3470574f6f4c99efe88a069079 annotatedSource NCIT_C98993 @default.
- B037b4d3470574f6f4c99efe88a069079 annotatedTarget "A rare syndrome that is characterized by the partial deletion of the long arm of chromosome 13. Signs and symptoms include low birth weight, craniofacial malformations, hands and feet malformations, and mental and psychomotor retardation." @default.