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- NCIT_C129973 IAO_0000115 "An autosomal dominant condition caused by mutation(s) in the SLC20A2 gene, encoding sodium-dependent phosphate transporter 2. It is characterized by calcification of the basal ganglia." @default.
- NCIT_C129973 NCIT_NHC0 "C129973" @default.
- NCIT_C129973 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C129973 NCIT_P108 "Idiopathic Basal Ganglia Calcification 1" @default.
- NCIT_C129973 NCIT_P207 "C0393590" @default.
- NCIT_C129973 NCIT_P322 "Cellosaurus" @default.
- NCIT_C129973 NCIT_R176 NCIT_C16612 @default.
- NCIT_C129973 NCIT_R176 NCIT_C189262 @default.
- NCIT_C129973 NCIT_R176 NCIT_C21295 @default.
- NCIT_C129973 NCIT_R176 NCIT_C28533 @default.
- NCIT_C129973 normalizedInformationContent "100" @default.
- NCIT_C129973 referenceCount "1" @default.
- NCIT_C129973 hasExactSynonym "BSPDC" @default.
- NCIT_C129973 hasExactSynonym "Bilateral Striopallidodentate Calcinosis" @default.
- NCIT_C129973 hasExactSynonym "IBGC1" @default.
- NCIT_C129973 hasExactSynonym "Idiopathic Basal Ganglia Calcification 1" @default.
- NCIT_C129973 inSubset NCIT_C165258 @default.
- NCIT_C129973 inSubset NCIT_C192842 @default.
- NCIT_C129973 type Class @default.
- NCIT_C129973 isDefinedBy ncit.owl @default.
- NCIT_C129973 label "Idiopathic Basal Ganglia Calcification 1" @default.
- NCIT_C129973 subClassOf B5dea61c1002668641a6dc6c7f28a27cb @default.
- NCIT_C129973 subClassOf Bf977770e07851b9a01aaddce6f236fa7 @default.
- NCIT_C129973 subClassOf NCIT_C129973 @default.
- NCIT_C129973 subClassOf NCIT_C2991 @default.
- NCIT_C129973 subClassOf NCIT_C4873 @default.
- NCIT_C129973 subClassOf NCIT_C53529 @default.
- NCIT_C129973 subClassOf NCIT_C53543 @default.
- NCIT_C129973 subClassOf NCIT_C53547 @default.
- NCIT_C129973 subClassOf NCIT_C7057 @default.