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- NCIT_C121565 IAO_0000115 "A rare autosomal recessive disorder associated with abnormalities in bone maturation, and lipids and hormone metabolism and characterized by intrauterine growth retardation, failure to thrive, short stature, a progeroid appearance, hypotonia, variable mental impairment, and death in childhood. Its cause is unknown." @default.
- NCIT_C121565 NCIT_NHC0 "C121565" @default.
- NCIT_C121565 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C121565 NCIT_P108 "Neonatal Progeroid Syndrome" @default.
- NCIT_C121565 NCIT_P207 "C0406586" @default.
- NCIT_C121565 NCIT_P322 "Cellosaurus" @default.
- NCIT_C121565 normalizedInformationContent "100" @default.
- NCIT_C121565 referenceCount "1" @default.
- NCIT_C121565 hasExactSynonym "Neonatal Progeroid Syndrome" @default.
- NCIT_C121565 hasExactSynonym "Wiedemann-Rautenstrauch Syndrome" @default.
- NCIT_C121565 inSubset NCIT_C165258 @default.
- NCIT_C121565 inSubset NCIT_C192842 @default.
- NCIT_C121565 type Class @default.
- NCIT_C121565 isDefinedBy ncit.owl @default.
- NCIT_C121565 label "Neonatal Progeroid Syndrome" @default.
- NCIT_C121565 subClassOf NCIT_C121565 @default.
- NCIT_C121565 subClassOf NCIT_C2991 @default.
- NCIT_C121565 subClassOf NCIT_C4873 @default.
- NCIT_C121565 subClassOf NCIT_C53529 @default.
- NCIT_C121565 subClassOf NCIT_C53543 @default.
- NCIT_C121565 subClassOf NCIT_C53547 @default.
- NCIT_C121565 subClassOf NCIT_C7057 @default.