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PubMed:10716718 JSONTXT

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PubMed_ArguminSci

Id Subject Object Predicate Lexical cue
T1 75-282 DRI_Background denotes Motor incoordination, immune deficiencies, and an increased risk of cancer are the characteristic features of the hereditary disease ataxia-telangiectasia (A-T), which is caused by mutations in the ATM gene.
T2 283-366 DRI_Approach denotes Through gene targeting, we have generated a line of Atm mutant mice, Atm(y/y) mice.
T3 367-500 DRI_Outcome denotes In contrast to other Atm mutant mice, Atm(y/y) mice show a lower incidence of thymic lymphoma and survive beyond a few months of age.
T4 501-587 DRI_Outcome denotes Atm(y/y) mice exhibit deficits in motor learning indicative of cerebellar dysfunction.
T5 588-763 DRI_Outcome denotes Even though we found no gross cerebellar degeneration in older Atm(y/y) animals, ectopic and abnormally differentiated Purkinje cells were apparent in mutant mice of all ages.
T6 764-888 DRI_Background denotes These findings establish that some neuropathological abnormalities seen in A-T patients also are present in Atm mutant mice.
T7 889-1018 DRI_Outcome denotes In addition, we report a previously unrecognized effect of Atm deficiency on development or maintenance of CD4(+)8(+) thymocytes.
T8 1019-1177 DRI_Challenge denotes We discuss these findings in the context of the hypothesis that abnormal development of Purkinje cells and lymphocytes contributes to the pathogenesis of A-T.

PMID_GLOBAL

Id Subject Object Predicate Lexical cue mondo_id
T1 189-207 DiseaseOrPhenotypicFeature denotes hereditary disease 0003847
T2 208-229 DiseaseOrPhenotypicFeature denotes ataxia-telangiectasia 0008840
T3 445-460 DiseaseOrPhenotypicFeature denotes thymic lymphoma 0000951
T4 618-641 DiseaseOrPhenotypicFeature denotes cerebellar degeneration 0022687

PubmedHPO

Id Subject Object Predicate Lexical cue
T1 81-95 HP_0002311 denotes incoordination
T2 97-116 HP_0002721 denotes immune deficiencies
T3 143-149 HP_0002664 denotes cancer
T4 208-214 HP_0001251 denotes ataxia
T5 215-229 HP_0001009 denotes telangiectasia
T6 452-460 HP_0002665 denotes lymphoma

NCBIDiseaseCorpus

Id Subject Object Predicate Lexical cue
T1 75-95 DiseaseClass:D002524 denotes Motor incoordination
T2 97-116 DiseaseClass:D007154 denotes immune deficiencies
T3 143-149 DiseaseClass:D009369 denotes cancer
T4 189-207 DiseaseClass:D030342 denotes hereditary disease
T5 208-229 SpecificDisease:D001260 denotes ataxia-telangiectasia
T6 231-234 SpecificDisease:D001260 denotes A-T
T7 445-460 SpecificDisease:D013953 denotes thymic lymphoma
T8 564-586 DiseaseClass:D002526 denotes cerebellar dysfunction
T9 618-641 DiseaseClass:D013132 denotes cerebellar degeneration
T10 799-830 DiseaseClass:D009422 denotes neuropathological abnormalities
T11 839-842 Modifier:D001260 denotes A-T
T12 948-962 SpecificDisease:OMIM:208900 denotes Atm deficiency
T13 1173-1176 SpecificDisease:D001260 denotes A-T

NCBI-Disease-Train

Id Subject Object Predicate Lexical cue database_id
T4889 75-95 DiseaseClass denotes Motor incoordination D002524
T4890 97-116 DiseaseClass denotes immune deficiencies D007154
T4891 143-149 DiseaseClass denotes cancer D009369
T4892 189-207 DiseaseClass denotes hereditary disease D030342
T4893 208-229 SpecificDisease denotes ataxia-telangiectasia D001260
T4894 231-234 SpecificDisease denotes A-T D001260
T4895 445-460 SpecificDisease denotes thymic lymphoma D013953
T4896 564-586 DiseaseClass denotes cerebellar dysfunction D002526
T4897 618-641 DiseaseClass denotes cerebellar degeneration D013132
T4898 799-830 DiseaseClass denotes neuropathological abnormalities D009422
T4899 839-842 Modifier denotes A-T D001260
T4900 948-962 SpecificDisease denotes Atm deficiency OMIM:208900
T4901 1173-1176 SpecificDisease denotes A-T D001260

NCBI-Disease-Corpus-All

Id Subject Object Predicate Lexical cue database_id
T4889 75-95 DiseaseClass denotes Motor incoordination D002524
T4890 97-116 DiseaseClass denotes immune deficiencies D007154
T4891 143-149 DiseaseClass denotes cancer D009369
T4892 189-207 DiseaseClass denotes hereditary disease D030342
T4893 208-229 SpecificDisease denotes ataxia-telangiectasia D001260
T4894 231-234 SpecificDisease denotes A-T D001260
T4895 445-460 SpecificDisease denotes thymic lymphoma D013953
T4896 564-586 DiseaseClass denotes cerebellar dysfunction D002526
T4897 618-641 DiseaseClass denotes cerebellar degeneration D013132
T4898 799-830 DiseaseClass denotes neuropathological abnormalities D009422
T4899 839-842 Modifier denotes A-T D001260
T4900 948-962 SpecificDisease denotes Atm deficiency OMIM:208900
T4901 1173-1176 SpecificDisease denotes A-T D001260

NCBI-Disease-Corpus-2stage-All

Id Subject Object Predicate Lexical cue
T1 143-149 DiseaseClass denotes cancer
T2 208-229 SpecificDisease denotes ataxia-telangiectasia
T3 231-234 SpecificDisease denotes A-T
T4 452-460 SpecificDisease denotes lymphoma
T5 839-842 SpecificDisease denotes A-T
T6 1173-1176 SpecificDisease denotes A-T

NCBI-Disease-Corpus-rezarta-All

Id Subject Object Predicate Lexical cue
T1 143-149 DiseaseClass denotes cancer
T2 208-229 SpecificDisease denotes ataxia-telangiectasia
T3 231-234 SpecificDisease denotes A-T
T4 452-460 SpecificDisease denotes lymphoma
T5 839-842 SpecificDisease denotes A-T
T6 1173-1176 SpecificDisease denotes A-T

NCBI-Disease-Corpus-4oGuideline-All

Id Subject Object Predicate Lexical cue
T1 58-73 Modifier denotes Atm mutant mice
T2 75-95 DiseaseClass denotes Motor incoordination
T3 97-116 DiseaseClass denotes immune deficiencies
T4 143-149 Modifier denotes cancer
T5 208-235 SpecificDisease denotes ataxia-telangiectasia (A-T)
T6 335-350 Modifier denotes Atm mutant mice
T7 352-365 Modifier denotes Atm(y/y) mice
T8 388-403 Modifier denotes Atm mutant mice
T9 405-418 Modifier denotes Atm(y/y) mice
T10 445-460 SpecificDisease denotes thymic lymphoma
T11 501-514 Modifier denotes Atm(y/y) mice
T12 535-549 DiseaseClass denotes motor learning
T13 564-586 DiseaseClass denotes cerebellar dysfunction
T14 618-641 DiseaseClass denotes cerebellar degeneration
T15 651-667 Modifier denotes Atm(y/y) animals
T16 839-851 SpecificDisease denotes A-T patients
T17 872-887 Modifier denotes Atm mutant mice
T18 948-962 Modifier denotes Atm deficiency
T19 1173-1176 Modifier denotes A-T

NCBI-Disease-Corpus-Simple-All

Id Subject Object Predicate Lexical cue
T1 0-8 Modifier denotes Abnormal
T2 24-73 SpecificDisease denotes Purkinje cells and lymphocytes in Atm mutant mice
T3 75-80 Modifier denotes Motor
T4 97-116 DiseaseClass denotes immune deficiencies
T5 125-134 Modifier denotes increased
T6 143-149 DiseaseClass denotes cancer
T7 200-235 SpecificDisease denotes disease ataxia-telangiectasia (A-T)
T8 273-281 SpecificDisease denotes ATM gene
T9 335-350 SpecificDisease denotes Atm mutant mice
T10 352-365 SpecificDisease denotes Atm(y/y) mice
T11 388-403 SpecificDisease denotes Atm mutant mice
T12 405-418 SpecificDisease denotes Atm(y/y) mice
T13 445-460 SpecificDisease denotes thymic lymphoma
T14 501-514 SpecificDisease denotes Atm(y/y) mice
T15 535-540 Modifier denotes motor
T16 564-586 SpecificDisease denotes cerebellar dysfunction
T17 618-641 SpecificDisease denotes cerebellar degeneration
T18 651-667 SpecificDisease denotes Atm(y/y) animals
T19 707-721 SpecificDisease denotes Purkinje cells
T20 739-750 SpecificDisease denotes mutant mice
T21 839-851 SpecificDisease denotes A-T patients
T22 872-887 SpecificDisease denotes Atm mutant mice
T23 948-962 SpecificDisease denotes Atm deficiency
T24 996-1017 SpecificDisease denotes CD4(+)8(+) thymocytes
T25 1083-1091 Modifier denotes abnormal
T26 1107-1137 SpecificDisease denotes Purkinje cells and lymphocytes
T27 1173-1176 SpecificDisease denotes A-T