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- B3c6dc5bf2df6e01b6a7b1256609016d3 NCIT_P378 "NCI" @default.
- B3c6dc5bf2df6e01b6a7b1256609016d3 type Axiom @default.
- B3c6dc5bf2df6e01b6a7b1256609016d3 annotatedProperty IAO_0000115 @default.
- B3c6dc5bf2df6e01b6a7b1256609016d3 annotatedSource NCIT_C66505 @default.
- B3c6dc5bf2df6e01b6a7b1256609016d3 annotatedTarget "A member of the class of histamine H2-receptor antagonists with antacid activity. Ranitidine is a competitive and reversible inhibitor of the action of histamine, released by enterochromaffin-like (ECL) cells, at the histamine H2-receptors on parietal cells in the stomach, thereby inhibiting the normal and meal-stimulated secretion of stomach acid. In addition, other substances that promote acid secretion have a reduced effect on parietal cells when the H2 receptors are blocked." @default.