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- B56c8d9c867fed6c35bcc170f9999360b NCIT_P378 "NCI" @default.
- B56c8d9c867fed6c35bcc170f9999360b type Axiom @default.
- B56c8d9c867fed6c35bcc170f9999360b annotatedProperty IAO_0000115 @default.
- B56c8d9c867fed6c35bcc170f9999360b annotatedSource NCIT_C19810 @default.
- B56c8d9c867fed6c35bcc170f9999360b annotatedTarget "Human DRD2 Gene at 11q23 encodes Dopamine Receptor D2, a G-protein coupled receptor that inhibits adenylyl cyclase activity. Missense mutation in DRD2 causes myoclonus dystonia; other mutations have been associated with schizophrenia. Alternative splicing results in two different isoforms. A third variant has been described, but it has not been determined whether this form is normal or due to aberrant splicing. Different alleles are associated with increased incidence of substance abuse. (NCI)" @default.