Matches in Ubergraph for { <http://purl.obolibrary.org/obo/NCIT_C185638> ?p ?o ?g. }
Showing items 1 to 27 of
27
with 100 items per page.
- NCIT_C185638 IAO_0000115 "A rare condition in which the two arms of chromosome 14 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_C185638 NCIT_NHC0 "C185638" @default.
- NCIT_C185638 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C185638 NCIT_P108 "Ring Chromosome 14 Syndrome" @default.
- NCIT_C185638 NCIT_P207 "C2930916" @default.
- NCIT_C185638 NCIT_P322 "Cellosaurus" @default.
- NCIT_C185638 NCIT_R174 NCIT_C12219 @default.
- NCIT_C185638 NCIT_R174 NCIT_C13202 @default.
- NCIT_C185638 NCIT_R174 NCIT_C13203 @default.
- NCIT_C185638 NCIT_R174 NCIT_C13209 @default.
- NCIT_C185638 NCIT_R174 NCIT_C13404 @default.
- NCIT_C185638 NCIT_R174 NCIT_C14134 @default.
- NCIT_C185638 NCIT_R174 NCIT_C21599 @default.
- NCIT_C185638 normalizedInformationContent "100" @default.
- NCIT_C185638 referenceCount "1" @default.
- NCIT_C185638 hasExactSynonym "Ring Chromosome 14 Syndrome" @default.
- NCIT_C185638 inSubset NCIT_C165258 @default.
- NCIT_C185638 inSubset NCIT_C192842 @default.
- NCIT_C185638 type Class @default.
- NCIT_C185638 isDefinedBy ncit.owl @default.
- NCIT_C185638 label "Ring Chromosome 14 Syndrome" @default.
- NCIT_C185638 subClassOf B1b1b0e534d029158b90d5294ca3a00b0 @default.
- NCIT_C185638 subClassOf B8e9b28be8f4a2c4b11b92307d24afdc5 @default.
- NCIT_C185638 subClassOf NCIT_C185638 @default.
- NCIT_C185638 subClassOf NCIT_C28193 @default.
- NCIT_C185638 subClassOf NCIT_C2991 @default.
- NCIT_C185638 subClassOf NCIT_C7057 @default.