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- Bcad04f02f2bb89192e7a3beca3c529ad NCIT_P378 "NCI" @default.
- Bcad04f02f2bb89192e7a3beca3c529ad type Axiom @default.
- Bcad04f02f2bb89192e7a3beca3c529ad annotatedProperty IAO_0000115 @default.
- Bcad04f02f2bb89192e7a3beca3c529ad annotatedSource NCIT_C3400 @default.
- Bcad04f02f2bb89192e7a3beca3c529ad annotatedTarget "A malignant neoplasm characterized by the chromosomal translocation t(X;18)(p11;q11). It can occur at any age, but mainly affects young adults, more commonly males. Although any site can be affected, the vast majority of the cases arise in the deep soft tissues of extremities, especially around the knee. Microscopically, synovial sarcoma is classified as monophasic (with a spindle or epithelial cell component) or biphasic (with both spindle and epithelial cell components). Synovial sarcomas can recur or metastasize to the lungs, bones, and lymph nodes." @default.