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- B4f6ef56fd9c83abfb83fe21b97f44637 NCIT_P378 "NICHD" @default.
- B4f6ef56fd9c83abfb83fe21b97f44637 type Axiom @default.
- B4f6ef56fd9c83abfb83fe21b97f44637 annotatedProperty NCIT_P325 @default.
- B4f6ef56fd9c83abfb83fe21b97f44637 annotatedSource NCIT_C3718 @default.
- B4f6ef56fd9c83abfb83fe21b97f44637 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.