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- NCIT_C75475 IAO_0000115 "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.
- NCIT_C75475 NCIT_NHC0 "C75475" @default.
- NCIT_C75475 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C75475 NCIT_P108 "Holoprosencephaly Type 4" @default.
- NCIT_C75475 NCIT_P207 "C1840528" @default.
- NCIT_C75475 NCIT_P366 "Holoprosencephaly_Type_4" @default.
- NCIT_C75475 NCIT_R176 NCIT_C16612 @default.
- NCIT_C75475 NCIT_R176 NCIT_C16615 @default.
- NCIT_C75475 NCIT_R176 NCIT_C20420 @default.
- NCIT_C75475 NCIT_R176 NCIT_C54362 @default.
- NCIT_C75475 NCIT_R176 NCIT_C75417 @default.
- NCIT_C75475 normalizedInformationContent "90.826665450122817" @default.
- NCIT_C75475 referenceCount "4" @default.
- NCIT_C75475 hasExactSynonym "Holoprosencephaly 4" @default.
- NCIT_C75475 hasExactSynonym "Holoprosencephaly Type 4" @default.
- NCIT_C75475 type Class @default.
- NCIT_C75475 isDefinedBy ncit.owl @default.
- NCIT_C75475 label "Holoprosencephaly Type 4" @default.
- NCIT_C75475 subClassOf B4144e3a5dbaa382aa281d83466ae0848 @default.
- NCIT_C75475 subClassOf Ba7176fcaf5c0bc870b1aae2dd28e3f86 @default.
- NCIT_C75475 subClassOf NCIT_C28193 @default.
- NCIT_C75475 subClassOf NCIT_C2991 @default.
- NCIT_C75475 subClassOf NCIT_C4873 @default.
- NCIT_C75475 subClassOf NCIT_C53529 @default.
- NCIT_C75475 subClassOf NCIT_C53543 @default.
- NCIT_C75475 subClassOf NCIT_C53547 @default.
- NCIT_C75475 subClassOf NCIT_C7057 @default.
- NCIT_C75475 subClassOf NCIT_C74988 @default.
- NCIT_C75475 subClassOf NCIT_C75475 @default.