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- Bd49a9300845704e43fb4096e9833312a hasDbXref "Orphanet:231230" @default.
- Bd49a9300845704e43fb4096e9833312a type Axiom @default.
- Bd49a9300845704e43fb4096e9833312a annotatedProperty IAO_0000115 @default.
- Bd49a9300845704e43fb4096e9833312a annotatedSource MONDO_0016488 @default.
- Bd49a9300845704e43fb4096e9833312a annotatedTarget "OBSOLETE. Beta-thalassemias associated with hemoglobin (Hb) anomalies result in a variable clinical spectrum, ranging from asymptomatic to severe, depending on the severity of the thalassemia mutation and on the type of the Hb anomaly [hereditary persistence of fetal Hb, delta-beta-thalassemia, Hb C - beta-thalassemia, Hb E - beta-thalassemia and Hb S - beta-thalassemia ]." @default.