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- Bcb774664aceb26750e81560d6974b4f6 NCIT_P378 "NICHD" @default.
- Bcb774664aceb26750e81560d6974b4f6 type Axiom @default.
- Bcb774664aceb26750e81560d6974b4f6 annotatedProperty NCIT_P325 @default.
- Bcb774664aceb26750e81560d6974b4f6 annotatedSource NCIT_C3718 @default.
- Bcb774664aceb26750e81560d6974b4f6 annotatedTarget "A syndrome characterized by a predisposition for Wilms tumor, aniridia, genitourinary anomalies, and developmental delay. This is a contiguous gene syndrome due to deletion in the vicinity of chromosome 11p13 in a region containing the WT1 and PAX6 genes." @default.