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- NCIT_C97569 IAO_0000115 "Human HOXA11 wild-type allele is located in the vicinity of 7p15.2 and is approximately 4 kb in length. This allele, which encodes homeobox protein Hox-A11, plays a role in transcriptional regulation. Mutation of the gene is associated with radioulnar synostosis with amegakaryocytic thrombocytopenia. Two chromosomal aberrations inv(7)(p15q34) and t(7;7)(p15;q34) of this gene and the TCRB gene locus lead to ectopic expression of the HOXA11 gene and are associated with T-cell acute lymphoblastic leukemia. A chromosomal translocation t(7;11)(p15;p15) of this gene and the NUP98 gene might be associated with chronic myelogenous leukemia." @default.
- NCIT_C97569 NCIT_NHC0 "C97569" @default.
- NCIT_C97569 NCIT_P100 "142958" @default.
- NCIT_C97569 NCIT_P102 "NM_005523" @default.
- NCIT_C97569 NCIT_P106 "Gene or Genome" @default.
- NCIT_C97569 NCIT_P107 "HOXA11 wt Allele" @default.
- NCIT_C97569 NCIT_P108 "HOXA11 wt Allele" @default.
- NCIT_C97569 NCIT_P207 "C3273496" @default.
- NCIT_C97569 NCIT_P321 "3207" @default.
- NCIT_C97569 NCIT_P322 "CTRP" @default.
- NCIT_C97569 NCIT_R37 NCIT_C16399 @default.
- NCIT_C97569 NCIT_R37 NCIT_C16879 @default.
- NCIT_C97569 NCIT_R37 NCIT_C17710 @default.
- NCIT_C97569 NCIT_R37 NCIT_C17828 @default.
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- NCIT_C97569 NCIT_R37 NCIT_C19077 @default.
- NCIT_C97569 NCIT_R37 NCIT_C19970 @default.
- NCIT_C97569 NCIT_R37 NCIT_C19986 @default.
- NCIT_C97569 NCIT_R37 NCIT_C20480 @default.
- NCIT_C97569 NCIT_R37 NCIT_C21049 @default.
- NCIT_C97569 NCIT_R37 NCIT_C21050 @default.
- NCIT_C97569 NCIT_R37 NCIT_C21124 @default.
- NCIT_C97569 NCIT_R37 NCIT_C21147 @default.
- NCIT_C97569 NCIT_R37 NCIT_C28498 @default.
- NCIT_C97569 NCIT_R37 NCIT_C40523 @default.
- NCIT_C97569 NCIT_R40 NCIT_C12219 @default.
- NCIT_C97569 NCIT_R40 NCIT_C13282 @default.
- NCIT_C97569 NCIT_R40 NCIT_C13377 @default.
- NCIT_C97569 NCIT_R40 NCIT_C13432 @default.
- NCIT_C97569 NCIT_R40 NCIT_C13446 @default.
- NCIT_C97569 NCIT_R40 NCIT_C14135 @default.
- NCIT_C97569 NCIT_R40 NCIT_C32221 @default.
- NCIT_C97569 NCIT_R40 NCIT_C34070 @default.
- NCIT_C97569 NCIT_R40 NCIT_C73640 @default.
- NCIT_C97569 NCIT_R41 NCIT_C14182 @default.
- NCIT_C97569 NCIT_R41 NCIT_C14225 @default.
- NCIT_C97569 NCIT_R41 NCIT_C14234 @default.
- NCIT_C97569 NCIT_R41 NCIT_C14250 @default.
- NCIT_C97569 NCIT_R41 NCIT_C14262 @default.
- NCIT_C97569 NCIT_R41 NCIT_C14282 @default.
- NCIT_C97569 NCIT_R41 NCIT_C25796 @default.
- NCIT_C97569 NCIT_R41 NCIT_C79740 @default.
- NCIT_C97569 normalizedInformationContent "100" @default.
- NCIT_C97569 referenceCount "1" @default.
- NCIT_C97569 hasExactSynonym "HOX1" @default.
- NCIT_C97569 hasExactSynonym "HOX1I" @default.
- NCIT_C97569 hasExactSynonym "HOXA11 wt Allele" @default.
- NCIT_C97569 hasExactSynonym "Homeo Box A11 Gene" @default.
- NCIT_C97569 hasExactSynonym "Homeobox A11 wt Allele" @default.
- NCIT_C97569 inSubset NCIT_C116977 @default.
- NCIT_C97569 inSubset NCIT_C142799 @default.
- NCIT_C97569 inSubset NCIT_C142800 @default.
- NCIT_C97569 type Class @default.
- NCIT_C97569 isDefinedBy ncit.owl @default.
- NCIT_C97569 label "HOXA11 wt Allele" @default.
- NCIT_C97569 subClassOf B345487f57c53b0669f6eaa4c81d514e9 @default.
- NCIT_C97569 subClassOf Bc04e88516cfe947b22a09bbd1c5e0a07 @default.
- NCIT_C97569 subClassOf NCIT_C105821 @default.
- NCIT_C97569 subClassOf NCIT_C16612 @default.
- NCIT_C97569 subClassOf NCIT_C16615 @default.
- NCIT_C97569 subClassOf NCIT_C20420 @default.
- NCIT_C97569 subClassOf NCIT_C54362 @default.
- NCIT_C97569 subClassOf NCIT_C97568 @default.
- NCIT_C97569 subClassOf NCIT_C97569 @default.