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PubMed:2491010 / 140-323 JSONTXT

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LitCoin-sentences

Id Subject Object Predicate Lexical cue
T2 0-183 Sentence denotes Eighty unrelated individuals with Duchenne muscular dystrophy (DMD) or Becker muscular dystrophy (BMD) were found to have deletions in the major deletion-rich region of the DMD locus.

LitCoin-entities

Id Subject Object Predicate Lexical cue db_id
86 34-61 DiseaseOrPhenotypicFeature denotes Duchenne muscular dystrophy MESH:D020388
87 63-66 DiseaseOrPhenotypicFeature denotes DMD MESH:D020388
88 71-96 DiseaseOrPhenotypicFeature denotes Becker muscular dystrophy MESH:D020388
89 98-101 DiseaseOrPhenotypicFeature denotes BMD MESH:D020388
90 173-176 GeneOrGeneProduct denotes DMD NCBIGene:1756

LitCoin_Mondo

Id Subject Object Predicate Lexical cue mondo_id
T3 34-61 DiseaseOrPhenotypicFeature denotes Duchenne muscular dystrophy 0010679
T4 43-61 DiseaseOrPhenotypicFeature denotes muscular dystrophy 0020121
T5 71-96 DiseaseOrPhenotypicFeature denotes Becker muscular dystrophy 0010311
T6 78-96 DiseaseOrPhenotypicFeature denotes muscular dystrophy 0020121

LitCoin-GeneOrGeneProduct-v0

Id Subject Object Predicate Lexical cue
T4 34-61 GeneOrGeneProduct denotes Duchenne muscular dystrophy
T5 63-66 GeneOrGeneProduct denotes DMD
T6 139-144 GeneOrGeneProduct denotes major
T7 154-158 GeneOrGeneProduct denotes rich
T8 173-176 GeneOrGeneProduct denotes DMD

LitCoin-GeneOrGeneProduct-v2

Id Subject Object Predicate Lexical cue
T4 34-61 GeneOrGeneProduct denotes Duchenne muscular dystrophy
T5 63-66 GeneOrGeneProduct denotes DMD
T6 139-144 GeneOrGeneProduct denotes major
T7 154-158 GeneOrGeneProduct denotes rich
T8 173-176 GeneOrGeneProduct denotes DMD

LitCoin-Disease-MeSH

Id Subject Object Predicate Lexical cue originalLabel
T3 34-61 DiseaseOrPhenotypicFeature denotes Duchenne muscular dystrophy D020388
T4 63-66 DiseaseOrPhenotypicFeature denotes DMD D020388
T5 71-96 DiseaseOrPhenotypicFeature denotes Becker muscular dystrophy D020388
T6 98-101 DiseaseOrPhenotypicFeature denotes BMD D020388
T7 173-176 DiseaseOrPhenotypicFeature denotes DMD D020388

LitCoin_Mondo_095

Id Subject Object Predicate Lexical cue mondo_id
T4 34-61 DiseaseOrPhenotypicFeature denotes Duchenne muscular dystrophy 0010679
T5 63-66 DiseaseOrPhenotypicFeature denotes DMD 0010679
T6 71-96 DiseaseOrPhenotypicFeature denotes Becker muscular dystrophy 0010311
T7 98-101 DiseaseOrPhenotypicFeature denotes BMD 0010311|0007931
T9 154-158 DiseaseOrPhenotypicFeature denotes rich 0015404
T10 173-176 DiseaseOrPhenotypicFeature denotes DMD 0010679

LitCoin-MeSH-Disease-2

Id Subject Object Predicate Lexical cue ID:
T3 34-61 DiseaseOrPhenotypicFeature denotes Duchenne muscular dystrophy D020388
T4 63-66 DiseaseOrPhenotypicFeature denotes DMD D020388
T5 71-96 DiseaseOrPhenotypicFeature denotes Becker muscular dystrophy D020388
T6 98-101 DiseaseOrPhenotypicFeature denotes BMD D020388
T7 173-176 DiseaseOrPhenotypicFeature denotes DMD D020388

LitCoin-MONDO_bioort2019

Id Subject Object Predicate Lexical cue #label
T3 34-61 DiseaseOrPhenotypicFeature denotes Duchenne muscular dystrophy D020388
T4 63-66 DiseaseOrPhenotypicFeature denotes DMD D020388
T5 71-96 DiseaseOrPhenotypicFeature denotes Becker muscular dystrophy D020388
T6 98-101 DiseaseOrPhenotypicFeature denotes BMD D020388
T7 173-176 DiseaseOrPhenotypicFeature denotes DMD D020388

LitCoin-training-merged

Id Subject Object Predicate Lexical cue #label
T7 173-176 DiseaseOrPhenotypicFeature denotes DMD D020388
T6 98-101 DiseaseOrPhenotypicFeature denotes BMD D020388
T5 71-96 DiseaseOrPhenotypicFeature denotes Becker muscular dystrophy D020388
T54900 63-66 DiseaseOrPhenotypicFeature denotes DMD D020388
T86623 34-61 DiseaseOrPhenotypicFeature denotes Duchenne muscular dystrophy D020388

PubmedHPO

Id Subject Object Predicate Lexical cue
T1 43-61 HP_0003560 denotes muscular dystrophy
T2 78-96 HP_0003560 denotes muscular dystrophy

NCBIDiseaseCorpus

Id Subject Object Predicate Lexical cue
T3 34-61 SpecificDisease:D020388 denotes Duchenne muscular dystrophy
T4 63-66 SpecificDisease:D020388 denotes DMD
T5 71-96 SpecificDisease:C537666 denotes Becker muscular dystrophy
T6 98-101 SpecificDisease:C537666 denotes BMD
T7 173-176 Modifier:D020388 denotes DMD