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- Ba145c8ba32bf5d9d2be194a38561ebe2 NCIT_P378 "NCI" @default.
- Ba145c8ba32bf5d9d2be194a38561ebe2 type Axiom @default.
- Ba145c8ba32bf5d9d2be194a38561ebe2 annotatedProperty IAO_0000115 @default.
- Ba145c8ba32bf5d9d2be194a38561ebe2 annotatedSource NCIT_C7541 @default.
- Ba145c8ba32bf5d9d2be194a38561ebe2 annotatedTarget "A malignant tumor that originates in the nuclear layer of the retina. As the most common primary tumor of the eye in children, retinoblastoma is still relatively uncommon, accounting for only 1% of all malignant tumors in pediatric patients. Approximately 95% of cases are diagnosed before age 5. These tumors may be multifocal, bilateral, congenital, inherited, or acquired. Seventy-five percent of retinoblastomas are unilateral; 60% occur sporadically. A predisposition to retinoblastoma has been associated with 13q14 cytogenetic abnormalities. Patients with the inherited form also appear to be at increased risk for secondary nonocular malignancies such as osteosarcoma, malignant fibrous histiocytoma, and fibrosarcoma." @default.