Matches in Ubergraph for { <http://purl.obolibrary.org/obo/NCIT_C53118> ?p ?o ?g. }
- NCIT_C53118 IAO_0000115 "Human RUNX1 wild-type allele is located in the vicinity of 21q22.3 and is approximately 262 kb in length. This allele, which encodes Runt-related transcription factor 1 protein, is involved in both the modulation of transcription by RNA polymerase II and in hematopoiesis. Chronic myelogenous leukemia with or without blastic crisis, acute non-lymphocytic leukemia, T-cell acute lymphocytic leukemia, and myelodysplastic syndrome are all associated with complex chromosomal rearrangements of this gene." @default.
- NCIT_C53118 NCIT_NHC0 "C53118" @default.
- NCIT_C53118 NCIT_P100 "151385" @default.
- NCIT_C53118 NCIT_P102 "NM_001754" @default.
- NCIT_C53118 NCIT_P106 "Gene or Genome" @default.
- NCIT_C53118 NCIT_P107 "RUNX1 wt Allele" @default.
- NCIT_C53118 NCIT_P108 "RUNX1 wt Allele" @default.
- NCIT_C53118 NCIT_P207 "C1705326" @default.
- NCIT_C53118 NCIT_P211 "ATP binding" @default.
- NCIT_C53118 NCIT_P211 "DNA binding" @default.
- NCIT_C53118 NCIT_P211 "biological_process unknown" @default.
- NCIT_C53118 NCIT_P211 "cellular_component unknown" @default.
- NCIT_C53118 NCIT_P211 "development" @default.
- NCIT_C53118 NCIT_P211 "molecular_function unknown" @default.
- NCIT_C53118 NCIT_P211 "nucleus" @default.
- NCIT_C53118 NCIT_P211 "regulation of transcription, DNA-dependent" @default.
- NCIT_C53118 NCIT_P211 "transcription factor activity" @default.
- NCIT_C53118 NCIT_P321 "861" @default.
- NCIT_C53118 NCIT_P322 "CTRP" @default.
- NCIT_C53118 NCIT_P366 "RUNX1_wt_Allele" @default.
- NCIT_C53118 NCIT_P96 "Core-Binding Factor Alpha" @default.
- NCIT_C53118 NCIT_P98 "The RUNX1 gene product binds to the core site, 5'-PYGPYGGT-3', of a number of enhancers and promoters (GeneCards)." @default.
- NCIT_C53118 NCIT_P98 "The translocation t(3;21)(q26;q22) of this gene and the EVI1 gene or the MDS1 gene are associated with myelodysplastic syndrome. The translocation t(1;21)(p36;q22) of this gene yields and the PRMD16 gene is associated with acute non-lymphocytic leukemia. The translocation t(12;21)(p12;q22) of this gene and the ETV6 gene is associated with B-cell acute lymphocytic leukemia (Atlas of Genetics and Cytogenetics in Hematology and Oncology)." @default.
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