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- NCIT_C2887 IAO_0000115 "Rare hereditary disease characterized by extreme sensitivity to ionizing radiation or radiomimetic drugs because of a defect in DNA repair. AT heterozygosity is estimated to occur in more than 2% of the U.S. population; heterozygotes exhibit increased radiation sensitivity and are at increased risk for several types of cancer. The normal version of the gene that is defective in AT appears to activate the p53-dependent response to DNA damage." @default.
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- NCIT_C2887 NCIT_A32 NCIT_C17103 @default.
- NCIT_C2887 NCIT_NHC0 "C2887" @default.
- NCIT_C2887 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C2887 NCIT_P107 "Ataxia Telangiectasia Syndrome" @default.
- NCIT_C2887 NCIT_P108 "Ataxia Telangiectasia Syndrome" @default.
- NCIT_C2887 NCIT_P207 "C0004135" @default.
- NCIT_C2887 NCIT_P322 "CCPS" @default.
- NCIT_C2887 NCIT_P322 "CTRP" @default.
- NCIT_C2887 NCIT_P322 "Cellosaurus" @default.
- NCIT_C2887 NCIT_P322 "GDC" @default.
- NCIT_C2887 NCIT_P325 "A rare, inherited, progressive, degenerative disease of childhood that causes loss of muscle control, a weakened immune system, and an increased risk of cancer." @default.
- NCIT_C2887 NCIT_P366 "Ataxia_Telangiectasia_Syndrome" @default.
- NCIT_C2887 NCIT_P375 "Ataxia-telangiectasia" @default.
- NCIT_C2887 NCIT_R106 NCIT_C36391 @default.
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- NCIT_C2887 NCIT_R106 NCIT_C97926 @default.
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- NCIT_C2887 NCIT_R108 NCIT_C3367 @default.
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- NCIT_C2887 NCIT_R108 NCIT_C54062 @default.
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- NCIT_C2887 NCIT_R176 NCIT_C16612 @default.
- NCIT_C2887 NCIT_R176 NCIT_C18583 @default.
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- NCIT_C2887 NCIT_R176 NCIT_C25870 @default.
- NCIT_C2887 NCIT_R176 NCIT_C25871 @default.
- NCIT_C2887 NCIT_R176 NCIT_C25872 @default.
- NCIT_C2887 NCIT_R176 NCIT_C25873 @default.
- NCIT_C2887 normalizedInformationContent "90.826665450122817" @default.
- NCIT_C2887 referenceCount "4" @default.
- NCIT_C2887 hasExactSynonym "Ataxia Telangiectasia Syndrome" @default.
- NCIT_C2887 hasExactSynonym "Ataxia Telangiectasia" @default.
- NCIT_C2887 hasExactSynonym "Ataxia-Telangiectasia Syndrome" @default.
- NCIT_C2887 hasExactSynonym "Ataxia-telangiectasia" @default.
- NCIT_C2887 hasExactSynonym "Louis-Bar Syndrome" @default.
- NCIT_C2887 hasExactSynonym "ataxia-telangiectasia" @default.
- NCIT_C2887 inSubset NCIT_C116977 @default.
- NCIT_C2887 inSubset NCIT_C118168 @default.
- NCIT_C2887 inSubset NCIT_C157711 @default.
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- NCIT_C2887 inSubset NCIT_C192842 @default.
- NCIT_C2887 type Class @default.
- NCIT_C2887 isDefinedBy ncit.owl @default.
- NCIT_C2887 label "Ataxia Telangiectasia Syndrome" @default.
- NCIT_C2887 subClassOf NCIT_C27351 @default.
- NCIT_C2887 subClassOf NCIT_C27551 @default.
- NCIT_C2887 subClassOf NCIT_C27871 @default.
- NCIT_C2887 subClassOf NCIT_C28193 @default.
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