Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Befc408f611b5ba62d09b7bc0cf4f08b4> ?p ?o ?g. }
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- Befc408f611b5ba62d09b7bc0cf4f08b4 NCIT_P378 "NCI" @default.
- Befc408f611b5ba62d09b7bc0cf4f08b4 type Axiom @default.
- Befc408f611b5ba62d09b7bc0cf4f08b4 annotatedProperty IAO_0000115 @default.
- Befc408f611b5ba62d09b7bc0cf4f08b4 annotatedSource NCIT_C84652 @default.
- Befc408f611b5ba62d09b7bc0cf4f08b4 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.