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- Bdf58f10da00d5bcd2df98ad8cf76efd3 NCIT_P378 "NCI" @default.
- Bdf58f10da00d5bcd2df98ad8cf76efd3 type Axiom @default.
- Bdf58f10da00d5bcd2df98ad8cf76efd3 annotatedProperty IAO_0000115 @default.
- Bdf58f10da00d5bcd2df98ad8cf76efd3 annotatedSource NCIT_C5183 @default.
- Bdf58f10da00d5bcd2df98ad8cf76efd3 annotatedTarget "Hereditary disorder transmitted by autosomal dominant genes (EXT1-3) and characterized by multiple exostoses (multiple osteochondromas) near the ends of long bones. The genetic abnormality results in a defect in the osteoclastic activity at the metaphyseal ends of the bone during the remodeling process in childhood or early adolescence. The metaphyses develop benign, bony outgrowths often capped by cartilage. A small number undergo neoplastic transformation." @default.