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- B598d0c411300f71188aaca9b416d66a4 NCIT_P378 "NCI" @default.
- B598d0c411300f71188aaca9b416d66a4 type Axiom @default.
- B598d0c411300f71188aaca9b416d66a4 annotatedProperty IAO_0000115 @default.
- B598d0c411300f71188aaca9b416d66a4 annotatedSource NCIT_C72070 @default.
- B598d0c411300f71188aaca9b416d66a4 annotatedTarget "A chronic disorder, possibly autoimmune, marked by excessive production of collagen which results in hardening and thickening of body tissues. The two types of systemic scleroderma, limited cutaneous and diffuse cutaneous are classified with focus on the extent of affected skin. A relationship exists between the extent of skin area affected and degree of internal organ/system involvement. Systemic scleroderma can manifest itself in pulmonary fibrosis, Raynaud's syndrome, digestive system telangiectasias, renal hypertension and/or pulmonary hypertension." @default.