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- NCIT_C179703 IAO_0000115 "A rare condition in which the two arms of chromosome 13 are fused resulting in a ring chromosome. Ring chromosome syndromes typically are characterized by developmental delay, intellectual disability, microcephaly, and dysmorphic facial features." @default.
- NCIT_C179703 NCIT_NHC0 "C179703" @default.
- NCIT_C179703 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C179703 NCIT_P108 "Ring Chromosome 13 Syndrome" @default.
- NCIT_C179703 NCIT_P208 "CL540813" @default.
- NCIT_C179703 NCIT_P322 "Cellosaurus" @default.
- NCIT_C179703 NCIT_R174 NCIT_C12219 @default.
- NCIT_C179703 NCIT_R174 NCIT_C13202 @default.
- NCIT_C179703 NCIT_R174 NCIT_C13203 @default.
- NCIT_C179703 NCIT_R174 NCIT_C13208 @default.
- NCIT_C179703 NCIT_R174 NCIT_C13404 @default.
- NCIT_C179703 NCIT_R174 NCIT_C14134 @default.
- NCIT_C179703 NCIT_R174 NCIT_C21599 @default.
- NCIT_C179703 normalizedInformationContent "100" @default.
- NCIT_C179703 referenceCount "1" @default.
- NCIT_C179703 hasExactSynonym "Ring Chromosome 13 Syndrome" @default.
- NCIT_C179703 inSubset NCIT_C165258 @default.
- NCIT_C179703 inSubset NCIT_C192842 @default.
- NCIT_C179703 type Class @default.
- NCIT_C179703 isDefinedBy ncit.owl @default.
- NCIT_C179703 label "Ring Chromosome 13 Syndrome" @default.
- NCIT_C179703 subClassOf B2de9418654021adcdd1593e927561006 @default.
- NCIT_C179703 subClassOf B7adaa09154a4bfab87bf356d32de358d @default.
- NCIT_C179703 subClassOf NCIT_C179703 @default.
- NCIT_C179703 subClassOf NCIT_C28193 @default.
- NCIT_C179703 subClassOf NCIT_C2991 @default.
- NCIT_C179703 subClassOf NCIT_C7057 @default.