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PubMed:18796596 JSONTXT 3 Projects

Annnotations TAB TSV DIC JSON TextAE Lectin_function IAV-Glycan

Id Subject Object Predicate Lexical cue mondo_id
T1 38-46 DiseaseOrPhenotypicFeature denotes myopathy 0005336
T2 98-121 DiseaseOrPhenotypicFeature denotes frontotemporal dementia 0010857|0017276
T4 123-126 DiseaseOrPhenotypicFeature denotes TAR 0010121
T5 211-235 DiseaseOrPhenotypicFeature denotes frontotemporal dementias 0010857|0017276
T7 237-240 DiseaseOrPhenotypicFeature denotes FTD 0010857|0017276
T9 257-260 DiseaseOrPhenotypicFeature denotes FTD 0010857|0017276
T11 357-365 DiseaseOrPhenotypicFeature denotes myopathy 0005336
T12 367-373 DiseaseOrPhenotypicFeature denotes IBMPFD 0000507
T13 382-388 DiseaseOrPhenotypicFeature denotes IBMPFD 0000507
T14 450-456 DiseaseOrPhenotypicFeature denotes IBMPFD 0000507
T15 515-521 DiseaseOrPhenotypicFeature denotes IBMPFD 0000507
T16 658-690 DiseaseOrPhenotypicFeature denotes sporadic inclusion body myositis 0007827
T17 692-696 DiseaseOrPhenotypicFeature denotes sIBM 0007827
T18 710-716 DiseaseOrPhenotypicFeature denotes IBMPFD 0000507
T19 721-725 DiseaseOrPhenotypicFeature denotes sIBM 0007827
T20 816-819 DiseaseOrPhenotypicFeature denotes FTD 0010857|0017276
T22 846-850 DiseaseOrPhenotypicFeature denotes sIBM 0007827
T23 855-891 DiseaseOrPhenotypicFeature denotes hereditary inclusion body myopathies 0007827