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- B41c7a477c164893e944b3b03a8d367db NCIT_P378 "NCI" @default.
- B41c7a477c164893e944b3b03a8d367db type Axiom @default.
- B41c7a477c164893e944b3b03a8d367db annotatedProperty IAO_0000115 @default.
- B41c7a477c164893e944b3b03a8d367db annotatedSource NCIT_C157449 @default.
- B41c7a477c164893e944b3b03a8d367db annotatedTarget "An autosomal dominant tumor syndrome caused by germline CDKN1B mutations that result in a phenotype similar to that of multiple endocrine neoplasia type 1, characterized by endocrine neoplasms, particularly in the parathyroid glands, pituitary, and pancreas. (WHO 2017)" @default.