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PubMed:21126715 JSONTXT 31 Projects

Annnotations TAB TSV DIC JSON TextAE

Id Subject Object Predicate Lexical cue mondo_id
T2 21-31 DiseaseOrPhenotypicFeature denotes congenital 0021140
T1 21-57 DiseaseOrPhenotypicFeature denotes congenital generalized lipodystrophy 0006536
T3 32-57 DiseaseOrPhenotypicFeature denotes generalized lipodystrophy 0027766
T4 44-57 DiseaseOrPhenotypicFeature denotes lipodystrophy 0006573
T5 116-152 DiseaseOrPhenotypicFeature denotes Congenital generalized lipodystrophy 0006536
T6 127-152 DiseaseOrPhenotypicFeature denotes generalized lipodystrophy 0027766
T7 139-152 DiseaseOrPhenotypicFeature denotes lipodystrophy 0006573
T8 164-168 DiseaseOrPhenotypicFeature denotes rare 0021136
T9 169-196 DiseaseOrPhenotypicFeature denotes autosomal recessive disease 0006025
T10 229-237 DiseaseOrPhenotypicFeature denotes complete 0700063
T11 507-521 DiseaseOrPhenotypicFeature denotes cardiomyopathy 0004994
T12 662-671 DiseaseOrPhenotypicFeature denotes xanthomas 0005236
T13 685-705 DiseaseOrPhenotypicFeature denotes hypertriglyceridemia 0005347
T14 916-923 DiseaseOrPhenotypicFeature denotes hepatic 0002251
T15 1006-1020 DiseaseOrPhenotypicFeature denotes cardiomyopathy 0004994