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- Bb5df0d35e58403b67b490e89afb0c9db NCIT_P378 "NCI" @default.
- Bb5df0d35e58403b67b490e89afb0c9db type Axiom @default.
- Bb5df0d35e58403b67b490e89afb0c9db annotatedProperty IAO_0000115 @default.
- Bb5df0d35e58403b67b490e89afb0c9db annotatedSource NCIT_C75475 @default.
- Bb5df0d35e58403b67b490e89afb0c9db annotatedTarget "A rare disorder caused by mutations in the TGIF gene mapped to chromosome 18p11.3. It is characterized by semilobar holoprosencephaly, hypotelorism, and ptosis." @default.