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- B8da991f0315affcec403b415e9a2c7d8 NCIT_P378 "NCI" @default.
- B8da991f0315affcec403b415e9a2c7d8 type Axiom @default.
- B8da991f0315affcec403b415e9a2c7d8 annotatedProperty IAO_0000115 @default.
- B8da991f0315affcec403b415e9a2c7d8 annotatedSource NCIT_C6727 @default.
- B8da991f0315affcec403b415e9a2c7d8 annotatedTarget "An autosomal dominant hereditary neoplastic syndrome. Two distinct clinicopathological entities are recognized: neurofibromatosis type 1 and neurofibromatosis type 2. Neurofibromatosis type 1 is associated with the presence of cafe-au-lait cutaneous lesions, multiple neurofibromas, malignant peripheral nerve sheath tumors, optic nerve gliomas, and bone lesions. Neurofibromatosis type 2 is associated with the presence of schwannomas, meningiomas, and gliomas." @default.