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- B456907b09b1acfa5a33b27fcdbcc0cae NCIT_P378 "NCI" @default.
- B456907b09b1acfa5a33b27fcdbcc0cae type Axiom @default.
- B456907b09b1acfa5a33b27fcdbcc0cae annotatedProperty IAO_0000115 @default.
- B456907b09b1acfa5a33b27fcdbcc0cae annotatedSource NCIT_C19810 @default.
- B456907b09b1acfa5a33b27fcdbcc0cae 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.