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- Bab1a95f54baae042d75c99c860d56888 NCIT_P378 "NCI" @default.
- Bab1a95f54baae042d75c99c860d56888 type Axiom @default.
- Bab1a95f54baae042d75c99c860d56888 annotatedProperty IAO_0000115 @default.
- Bab1a95f54baae042d75c99c860d56888 annotatedSource NCIT_C84652 @default.
- Bab1a95f54baae042d75c99c860d56888 annotatedTarget "A genetic syndrome caused by mutations in the HRAS gene. It is characterized by developmental delay, mental retardation, loose skin folds, cardiomyopathy, tachycardia, and structural heart defects. Patients are at an increased risk of developing benign or malignant neoplasms." @default.