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- B19e703f57d89fb4b25619f28a73568fc hasDbXref "Orphanet:431353" @default.
- B19e703f57d89fb4b25619f28a73568fc hasDbXref "https://orcid.org/0000-0001-5208-3432" @default.
- B19e703f57d89fb4b25619f28a73568fc type Axiom @default.
- B19e703f57d89fb4b25619f28a73568fc annotatedProperty IAO_0000115 @default.
- B19e703f57d89fb4b25619f28a73568fc annotatedSource MONDO_0018554 @default.
- B19e703f57d89fb4b25619f28a73568fc annotatedTarget "A rare subgroup of pulmonary arterial hypertension (PAH) characterized by obliterative fibrosis of the small pulmonary veins and venules and/or capillary infiltration of the pulmonary interstitium leading to increased pulmonary vascular resistance and right ventricular dysfunction." @default.