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- NCIT_C165729 IAO_0000115 "A deletion of chromosomal material at 17p13.1. This chromosomal aberration includes deletion of the TP53 gene and is associated with chronic lymphocytic leukemia." @default.
- NCIT_C165729 NCIT_NHC0 "C165729" @default.
- NCIT_C165729 NCIT_P106 "Cell or Molecular Dysfunction" @default.
- NCIT_C165729 NCIT_P107 "del(17p13.1)" @default.
- NCIT_C165729 NCIT_P108 "del(17p13.1)" @default.
- NCIT_C165729 NCIT_P208 "CL978880" @default.
- NCIT_C165729 NCIT_P322 "CTRP" @default.
- NCIT_C165729 NCIT_R173 NCIT_C12219 @default.
- NCIT_C165729 NCIT_R173 NCIT_C13202 @default.
- NCIT_C165729 NCIT_R173 NCIT_C13203 @default.
- NCIT_C165729 NCIT_R173 NCIT_C13212 @default.
- NCIT_C165729 NCIT_R173 NCIT_C13404 @default.
- NCIT_C165729 NCIT_R173 NCIT_C14134 @default.
- NCIT_C165729 NCIT_R173 NCIT_C21599 @default.
- NCIT_C165729 normalizedInformationContent "100" @default.
- NCIT_C165729 referenceCount "1" @default.
- NCIT_C165729 hasExactSynonym "-17p13.1" @default.
- NCIT_C165729 hasExactSynonym "17p13.1 Deletion" @default.
- NCIT_C165729 hasExactSynonym "del(17)(p13.1)" @default.
- NCIT_C165729 hasExactSynonym "del(17p13.1)" @default.
- NCIT_C165729 inSubset NCIT_C116977 @default.
- NCIT_C165729 inSubset NCIT_C142799 @default.
- NCIT_C165729 inSubset NCIT_C142800 @default.
- NCIT_C165729 type Class @default.
- NCIT_C165729 isDefinedBy ncit.owl @default.
- NCIT_C165729 label "del(17p13.1)" @default.
- NCIT_C165729 subClassOf NCIT_C129438 @default.
- NCIT_C165729 subClassOf NCIT_C165729 @default.
- NCIT_C165729 subClassOf NCIT_C171053 @default.
- NCIT_C165729 subClassOf NCIT_C2950 @default.
- NCIT_C165729 subClassOf NCIT_C36541 @default.
- NCIT_C165729 subClassOf NCIT_C3910 @default.
- NCIT_C165729 subClassOf NCIT_C9484 @default.