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- B98ff03dea1438f44b0adfdd8d12fdc4b NCIT_P378 "NCI" @default.
- B98ff03dea1438f44b0adfdd8d12fdc4b type Axiom @default.
- B98ff03dea1438f44b0adfdd8d12fdc4b annotatedProperty IAO_0000115 @default.
- B98ff03dea1438f44b0adfdd8d12fdc4b annotatedSource NCIT_C2989 @default.
- B98ff03dea1438f44b0adfdd8d12fdc4b annotatedTarget "A congenital anomaly characterized by immunodeficiency, abnormal facies, congenital heart disease, hypocalcemia, and increased susceptibility to infections. Pathologic characteristics include conotruncal abnormalities and absence or hypoplasia of thymus and parathyroid glands. DiGeorge syndrome is associated with abnormalities of chromosome 22. Also known as DiGeorge anomaly." @default.