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- B8e772b044d5ffa7a92bbf31d152c1d17 hasDbXref "NCIT:C9222" @default.
- B8e772b044d5ffa7a92bbf31d152c1d17 type Axiom @default.
- B8e772b044d5ffa7a92bbf31d152c1d17 annotatedProperty IAO_0000115 @default.
- B8e772b044d5ffa7a92bbf31d152c1d17 annotatedSource MONDO_0003789 @default.
- B8e772b044d5ffa7a92bbf31d152c1d17 annotatedTarget "A familial carcinoma inherited in an autosomal dominant trait. It is characterized by the development of multiple, bilateral papillary renal cell carcinomas. The carcinomas range from microscopic lesions to clinically symptomatic tumors. It is associated with activating mutations of the MET oncogene." @default.