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- B00da799e65ef69302aa79f3d6f2bc60e NCIT_P378 "NICHD" @default.
- B00da799e65ef69302aa79f3d6f2bc60e type Axiom @default.
- B00da799e65ef69302aa79f3d6f2bc60e annotatedProperty NCIT_P325 @default.
- B00da799e65ef69302aa79f3d6f2bc60e annotatedSource NCIT_C84668 @default.
- B00da799e65ef69302aa79f3d6f2bc60e annotatedTarget "A Wilms tumor 1 gene syndrome caused by various point mutation(s) affecting the zinc finger(s) of the Wilms tumor protein. This syndrome is characterized by congenital nephropathy (diffuse mesangial sclerosis), gonadal dysgenesis resulting in atypical genital and reproductive tract development in male infants, and high risk for development of Wilms tumor, an embryonal neoplasm defined by the presence of epithelial, mesenchymal, and blastema components." @default.