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- NCIT_C153178 IAO_0000115 "A condition caused by mutation(s) in the RAD50 gene, encoding DNA repair protein RAD50. It is characterized by microcephaly and chromosomal instability." @default.
- NCIT_C153178 NCIT_NHC0 "C153178" @default.
- NCIT_C153178 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C153178 NCIT_P108 "Nijmegen Breakage Syndrome-Like Disorder" @default.
- NCIT_C153178 NCIT_P207 "C2751318" @default.
- NCIT_C153178 NCIT_P322 "Cellosaurus" @default.
- NCIT_C153178 NCIT_R176 NCIT_C104708 @default.
- NCIT_C153178 NCIT_R176 NCIT_C153246 @default.
- NCIT_C153178 NCIT_R176 NCIT_C16612 @default.
- NCIT_C153178 NCIT_R176 NCIT_C19676 @default.
- NCIT_C153178 normalizedInformationContent "100" @default.
- NCIT_C153178 referenceCount "1" @default.
- NCIT_C153178 hasExactSynonym "NBSLD" @default.
- NCIT_C153178 hasExactSynonym "Nijmegen Breakage Syndrome-Like Disorder" @default.
- NCIT_C153178 hasExactSynonym "RAD50 Deficiency" @default.
- NCIT_C153178 inSubset NCIT_C165258 @default.
- NCIT_C153178 inSubset NCIT_C192842 @default.
- NCIT_C153178 type Class @default.
- NCIT_C153178 isDefinedBy ncit.owl @default.
- NCIT_C153178 label "Nijmegen Breakage Syndrome-Like Disorder" @default.
- NCIT_C153178 subClassOf B94cf99fd04db91cefb06ad9520de47ed @default.
- NCIT_C153178 subClassOf Ba62b2b53ad9ca6df7f12e2690473075c @default.
- NCIT_C153178 subClassOf NCIT_C153178 @default.
- NCIT_C153178 subClassOf NCIT_C2991 @default.
- NCIT_C153178 subClassOf NCIT_C3101 @default.
- NCIT_C153178 subClassOf NCIT_C7057 @default.
- NCIT_C153178 subClassOf NCIT_C7757 @default.