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- B3a56278fcf03237673d35af62956ab9f NCIT_P378 "NCI" @default.
- B3a56278fcf03237673d35af62956ab9f type Axiom @default.
- B3a56278fcf03237673d35af62956ab9f annotatedProperty IAO_0000115 @default.
- B3a56278fcf03237673d35af62956ab9f annotatedSource NCIT_C157461 @default.
- B3a56278fcf03237673d35af62956ab9f annotatedTarget "An extremely rare autosomal recessive inherited disorder caused by mutations in the GCGR gene. It is characterized by the presence of islet glucagon cell hyperplasia and glucagon cell tumors." @default.