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- B5d1b6f486febe2b740cbfeeb1f842611 NCIT_P378 "NCI" @default.
- B5d1b6f486febe2b740cbfeeb1f842611 type Axiom @default.
- B5d1b6f486febe2b740cbfeeb1f842611 annotatedProperty IAO_0000115 @default.
- B5d1b6f486febe2b740cbfeeb1f842611 annotatedSource NCIT_C61877 @default.
- B5d1b6f486febe2b740cbfeeb1f842611 annotatedTarget "The sodium salt form of a substituted benzimidazole with proton pump inhibitor activity. Pantoprazole is a lipophilic, weak base that crosses the parietal cell membrane and enters the acidic parietal cell canaliculus where it becomes protonated, producing the active metabolite sulfenamide, which forms an irreversible covalent bond with two sites of the H+/K+-ATPase enzyme located on the gastric parietal cell, thereby inhibiting both basal and stimulated gastric acid production." @default.