Matches in Ubergraph for { <http://purl.obolibrary.org/obo/NCIT_C169001> ?p ?o ?g. }
Showing items 1 to 27 of
27
with 100 items per page.
- NCIT_C169001 IAO_0000115 "A rare condition in which the two arms of chromosome 20 are fused resulting in a ring chromosome. It is characterized by recurrent seizures with an onset in childhood. Additional features my include microcephaly and short stature." @default.
- NCIT_C169001 NCIT_NHC0 "C169001" @default.
- NCIT_C169001 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C169001 NCIT_P108 "Ring Chromosome 20 Syndrome" @default.
- NCIT_C169001 NCIT_P207 "C0265482" @default.
- NCIT_C169001 NCIT_P322 "Cellosaurus" @default.
- NCIT_C169001 NCIT_R174 NCIT_C12219 @default.
- NCIT_C169001 NCIT_R174 NCIT_C13202 @default.
- NCIT_C169001 NCIT_R174 NCIT_C13203 @default.
- NCIT_C169001 NCIT_R174 NCIT_C13216 @default.
- NCIT_C169001 NCIT_R174 NCIT_C13404 @default.
- NCIT_C169001 NCIT_R174 NCIT_C14134 @default.
- NCIT_C169001 NCIT_R174 NCIT_C21599 @default.
- NCIT_C169001 normalizedInformationContent "100" @default.
- NCIT_C169001 referenceCount "1" @default.
- NCIT_C169001 hasExactSynonym "Ring Chromosome 20 Syndrome" @default.
- NCIT_C169001 inSubset NCIT_C165258 @default.
- NCIT_C169001 inSubset NCIT_C192842 @default.
- NCIT_C169001 type Class @default.
- NCIT_C169001 isDefinedBy ncit.owl @default.
- NCIT_C169001 label "Ring Chromosome 20 Syndrome" @default.
- NCIT_C169001 subClassOf Bc2db81b343c437e1dfd3bfe68cb9508e @default.
- NCIT_C169001 subClassOf Be4b0b0687afbd77d05473121df1acca4 @default.
- NCIT_C169001 subClassOf NCIT_C169001 @default.
- NCIT_C169001 subClassOf NCIT_C28193 @default.
- NCIT_C169001 subClassOf NCIT_C2991 @default.
- NCIT_C169001 subClassOf NCIT_C7057 @default.