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Matches in Ubergraph for { <http://purl.obolibrary.org/obo/NCIT_C3274> ?p ?o ?g. }

• NCIT_C3274 IAO_0000115 "An autosomal dominant disorder caused by mutations in the NF2 tumor suppressor gene. It is characterized by the development of peripheral and central nervous system tumors including acoustic schwannomas, neurofibromas, gliomas, and meningiomas." @default.
• NCIT_C3274 NCIT_A13 NCIT_C17425 @default.
• NCIT_C3274 NCIT_NHC0 "C3274" @default.
• NCIT_C3274 NCIT_P106 "Disease or Syndrome" @default.
• NCIT_C3274 NCIT_P107 "Neurofibromatosis Type 2" @default.
• NCIT_C3274 NCIT_P108 "Neurofibromatosis Type 2" @default.
• NCIT_C3274 NCIT_P207 "C0027832" @default.
• NCIT_C3274 NCIT_P322 "CCPS" @default.
• NCIT_C3274 NCIT_P322 "CPTAC" @default.
• NCIT_C3274 NCIT_P322 "CTRP" @default.
• NCIT_C3274 NCIT_P322 "Cellosaurus" @default.
• NCIT_C3274 NCIT_P322 "PCDC" @default.
• NCIT_C3274 NCIT_P325 "A genetic condition in which tumors form on the nerves of the inner ear and cause loss of hearing and balance. Tumors may also occur in the brain and on nerves in the skull and spinal cord, and may cause loss of speech, eye movement, and the ability to swallow." @default.
• NCIT_C3274 NCIT_P366 "Neurofibromatosis_Type_2" @default.
• NCIT_C3274 NCIT_P375 "Neurofibromatosis, type 2 [acoustic neurofibromatosis]" @default.
• NCIT_C3274 NCIT_R106 NCIT_C178119 @default.
• NCIT_C3274 NCIT_R106 NCIT_C36327 @default.
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• NCIT_C3274 NCIT_R126 NCIT_C118420 @default.
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• NCIT_C3274 NCIT_R126 NCIT_C27166 @default.

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