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- NCIT_C123437 IAO_0000115 "A rare, autosomal recessive inherited syndrome caused by mutations in the MMP2 gene. It is characterized by the presence of multiple, painless subcutaneous nodules, osteolysis particularly in the hands and feet, osteoporosis, and arthropathy." @default.
- NCIT_C123437 NCIT_NHC0 "C123437" @default.
- NCIT_C123437 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C123437 NCIT_P108 "Multicentric Osteolysis, Nodulosis, and Arthropathy" @default.
- NCIT_C123437 NCIT_P207 "C1850155" @default.
- NCIT_C123437 NCIT_R176 NCIT_C16612 @default.
- NCIT_C123437 NCIT_R176 NCIT_C21275 @default.
- NCIT_C123437 NCIT_R176 NCIT_C21281 @default.
- NCIT_C123437 NCIT_R176 NCIT_C25804 @default.
- NCIT_C123437 NCIT_R176 NCIT_C26003 @default.
- NCIT_C123437 NCIT_R176 NCIT_C26514 @default.
- NCIT_C123437 normalizedInformationContent "100" @default.
- NCIT_C123437 referenceCount "1" @default.
- NCIT_C123437 hasExactSynonym "Hereditary Multicentric Osteolysis" @default.
- NCIT_C123437 hasExactSynonym "MONA" @default.
- NCIT_C123437 hasExactSynonym "Multicentric Osteolysis, Nodulosis, and Arthropathy" @default.
- NCIT_C123437 type Class @default.
- NCIT_C123437 isDefinedBy ncit.owl @default.
- NCIT_C123437 label "Multicentric Osteolysis, Nodulosis, and Arthropathy" @default.
- NCIT_C123437 subClassOf B718f520907d0e5732a97a3cecf47aff5 @default.
- NCIT_C123437 subClassOf Bf2d4b68147a5d4ef75ac8c8350023d4e @default.
- NCIT_C123437 subClassOf NCIT_C123437 @default.
- NCIT_C123437 subClassOf NCIT_C170732 @default.
- NCIT_C123437 subClassOf NCIT_C28193 @default.
- NCIT_C123437 subClassOf NCIT_C2991 @default.
- NCIT_C123437 subClassOf NCIT_C4873 @default.
- NCIT_C123437 subClassOf NCIT_C53529 @default.
- NCIT_C123437 subClassOf NCIT_C53543 @default.
- NCIT_C123437 subClassOf NCIT_C53547 @default.
- NCIT_C123437 subClassOf NCIT_C7057 @default.