Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Bf3ee8d3fd6b1b2ea299b1f74865e74a9> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- Bf3ee8d3fd6b1b2ea299b1f74865e74a9 NCIT_P378 "ACC/AHA" @default.
- Bf3ee8d3fd6b1b2ea299b1f74865e74a9 type Axiom @default.
- Bf3ee8d3fd6b1b2ea299b1f74865e74a9 annotatedProperty NCIT_P325 @default.
- Bf3ee8d3fd6b1b2ea299b1f74865e74a9 annotatedSource NCIT_C75006 @default.
- Bf3ee8d3fd6b1b2ea299b1f74865e74a9 annotatedTarget "A genetic syndrome characterized by a rare autosomal dominant syndrome caused by mutations in the TGFBR1 or TGFBR2 genes. It is characterized by aortic dilation and dissection, vascular tortuosity, hypertelorism, bifid uvula, scoliosis, and pectus deformities." @default.