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- NCIT_C101039 IAO_0000115 "A rare congenital disorder, this is the non-lethal variant of multiple pterygium syndrome, characterized by orthopedic and craniofacial abnormalities, pterygium and akinethesia. The majority of cases are autosomal dominant." @default.
- NCIT_C101039 NCIT_NHC0 "C101039" @default.
- NCIT_C101039 NCIT_P106 "Congenital Abnormality" @default.
- NCIT_C101039 NCIT_P108 "Escobar Syndrome" @default.
- NCIT_C101039 NCIT_P207 "C0265261" @default.
- NCIT_C101039 NCIT_P322 "NICHD" @default.
- NCIT_C101039 normalizedInformationContent "100" @default.
- NCIT_C101039 referenceCount "1" @default.
- NCIT_C101039 hasExactSynonym "Escobar Syndrome" @default.
- NCIT_C101039 inSubset NCIT_C90259 @default.
- NCIT_C101039 inSubset NCIT_C99147 @default.
- NCIT_C101039 type Class @default.
- NCIT_C101039 isDefinedBy ncit.owl @default.
- NCIT_C101039 label "Escobar Syndrome" @default.
- NCIT_C101039 subClassOf NCIT_C101039 @default.
- NCIT_C101039 subClassOf NCIT_C28193 @default.
- NCIT_C101039 subClassOf NCIT_C2849 @default.
- NCIT_C101039 subClassOf NCIT_C2991 @default.
- NCIT_C101039 subClassOf NCIT_C36287 @default.
- NCIT_C101039 subClassOf NCIT_C53529 @default.
- NCIT_C101039 subClassOf NCIT_C53547 @default.
- NCIT_C101039 subClassOf NCIT_C7057 @default.
- NCIT_C101039 subClassOf NCIT_C97151 @default.