Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Bfffcc93cc5be26262b8a79c12d61b122> ?p ?o ?g. }
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- Bfffcc93cc5be26262b8a79c12d61b122 hasDbXref 0000-0002-0736-9199 @default.
- Bfffcc93cc5be26262b8a79c12d61b122 type Axiom @default.
- Bfffcc93cc5be26262b8a79c12d61b122 annotatedProperty IAO_0000115 @default.
- Bfffcc93cc5be26262b8a79c12d61b122 annotatedSource HP_0001057 @default.
- Bfffcc93cc5be26262b8a79c12d61b122 annotatedTarget "A developmental defect resulting in the congenital absence of skin in multiple or solitary non-inflammatory, well-demarcated, oval or circular ulcers with a diameter of about 1 to 2 cm. Aplasia cutis congenita most commonly occurs on the scalp, but may present in the face, trunk, or limbs." @default.