Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Bfa53576cbc482aa3a3988a93e1cb047e> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- Bfa53576cbc482aa3a3988a93e1cb047e NCIT_P378 "NICHD" @default.
- Bfa53576cbc482aa3a3988a93e1cb047e type Axiom @default.
- Bfa53576cbc482aa3a3988a93e1cb047e annotatedProperty NCIT_P325 @default.
- Bfa53576cbc482aa3a3988a93e1cb047e annotatedSource NCIT_C7541 @default.
- Bfa53576cbc482aa3a3988a93e1cb047e 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.