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- NCIT_C75481 IAO_0000115 "An X-linked inherited syndrome caused by mutations in the OFD1 gene mapped to chromosome Xp22.2. It is characterized by malformations of the face, oral cavity, and fingers." @default.
- NCIT_C75481 NCIT_NHC0 "C75481" @default.
- NCIT_C75481 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C75481 NCIT_P108 "Orofaciodigital Syndrome Type 1" @default.
- NCIT_C75481 NCIT_P208 "CL554670" @default.
- NCIT_C75481 NCIT_P366 "Orofaciodigital_Syndrome_Type_1" @default.
- NCIT_C75481 NCIT_R176 NCIT_C16612 @default.
- NCIT_C75481 NCIT_R176 NCIT_C20194 @default.
- NCIT_C75481 NCIT_R176 NCIT_C75879 @default.
- NCIT_C75481 normalizedInformationContent "100" @default.
- NCIT_C75481 referenceCount "1" @default.
- NCIT_C75481 hasExactSynonym "Orofaciodigital Syndrome Type 1" @default.
- NCIT_C75481 type Class @default.
- NCIT_C75481 isDefinedBy ncit.owl @default.
- NCIT_C75481 label "Orofaciodigital Syndrome Type 1" @default.
- NCIT_C75481 subClassOf B097d3de174ccca5e3c641c0fdc9c07ff @default.
- NCIT_C75481 subClassOf B0fd4769e63eeddeff040c39181be87f5 @default.
- NCIT_C75481 subClassOf NCIT_C28193 @default.
- NCIT_C75481 subClassOf NCIT_C2991 @default.
- NCIT_C75481 subClassOf NCIT_C4873 @default.
- NCIT_C75481 subClassOf NCIT_C53529 @default.
- NCIT_C75481 subClassOf NCIT_C53543 @default.
- NCIT_C75481 subClassOf NCIT_C53547 @default.
- NCIT_C75481 subClassOf NCIT_C7057 @default.
- NCIT_C75481 subClassOf NCIT_C75481 @default.