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PubMed:15122708 JSONTXT 11 Projects

Annnotations TAB TSV DIC JSON TextAE

Id Subject Object Predicate Lexical cue #label ID: cellosaurus_accession_id
T87659 0-6 GeneOrGeneProduct denotes Desmin
T1 0-41 DiseaseOrPhenotypicFeature denotes Desmin-related myopathy with Mallory body C535683
T56406 88-101 ChemicalEntity denotes selenoprotein http://purl.obolibrary.org/obo/CHEBI_80757
T66366 88-103 GeneOrGeneProduct denotes selenoprotein N
T22768 110-116 GeneOrGeneProduct denotes Desmin
T2 110-135 DiseaseOrPhenotypicFeature denotes Desmin-related myopathies C563319
T3 137-141 DiseaseOrPhenotypicFeature denotes DRMs C563319
T4 172-188 DiseaseOrPhenotypicFeature denotes muscle disorders D009135
T82381 249-255 GeneOrGeneProduct denotes desmin
T38213 274-280 GeneOrGeneProduct denotes desmin
T68109 289-307 GeneOrGeneProduct denotes alpha-B crystallin
T77232 357-360 CellLine denotes DRM CVCL_1G81
T5 498-500 DiseaseOrPhenotypicFeature denotes MB DISEASE
T6 501-505 DiseaseOrPhenotypicFeature denotes DRMs C563319
T22421 547-555 OrganismTaxon denotes patients
T33937 585-598 ChemicalEntity denotes selenoprotein http://purl.obolibrary.org/obo/CHEBI_80757
T17249 585-600 GeneOrGeneProduct denotes selenoprotein N
T31521 607-612 GeneOrGeneProduct denotes SEPN1
T7 646-654 DiseaseOrPhenotypicFeature denotes myopathy D009135
T8 687-695 DiseaseOrPhenotypicFeature denotes myopathy D009135
T9 766-784 DiseaseOrPhenotypicFeature denotes muscular dystrophy D009136
T10 818-839 DiseaseOrPhenotypicFeature denotes multiminicore disease C564969
T11 973-975 DiseaseOrPhenotypicFeature denotes MB DISEASE
T85636 976-979 CellLine denotes DRM CVCL_1G81
T14435 984-989 GeneOrGeneProduct denotes SEPN1
T12 1007-1009 DiseaseOrPhenotypicFeature denotes MB DISEASE
T2801 1010-1013 CellLine denotes DRM CVCL_1G81
T96348 1077-1082 GeneOrGeneProduct denotes SEPN1
T52223 1127-1132 GeneOrGeneProduct denotes SEPN1
T80174 1186-1194 OrganismTaxon denotes patients
T13 1235-1237 DiseaseOrPhenotypicFeature denotes MB DISEASE
T87186 1238-1241 CellLine denotes DRM CVCL_1G81
T14 1316-1318 DiseaseOrPhenotypicFeature denotes MB DISEASE
T24812 1319-1322 CellLine denotes DRM CVCL_1G81
T84250 1416-1419 CellLine denotes DRM CVCL_1G81
T15 1551-1561 DiseaseOrPhenotypicFeature denotes myopathies D009135