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PubMed:22549782 / 151-303 JSONTXT

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Inflammaging

Id Subject Object Predicate Lexical cue
T2 0-152 Sentence denotes Duchenne muscular dystrophy (DMD) is a genetic disorder caused by dystrophin mutations, characterized by chronic inflammation and severe muscle wasting.
T2 0-152 Sentence denotes Duchenne muscular dystrophy (DMD) is a genetic disorder caused by dystrophin mutations, characterized by chronic inflammation and severe muscle wasting.

Glycosmos6-MAT

Id Subject Object Predicate Lexical cue
T1 137-143 http://purl.obolibrary.org/obo/MAT_0000025 denotes muscle

PubmedHPO

Id Subject Object Predicate Lexical cue
T1 9-27 HP_0003560 denotes muscular dystrophy

Allie

Id Subject Object Predicate Lexical cue
SS1_22549782_1_0 0-27 expanded denotes Duchenne muscular dystrophy
SS2_22549782_1_0 29-32 abbr denotes DMD
AE1_22549782_1_0 SS1_22549782_1_0 SS2_22549782_1_0 abbreviatedTo Duchenne muscular dystrophy,DMD

GlyCosmos600-FMA

Id Subject Object Predicate Lexical cue fma_id
T2 66-76 Body_part denotes dystrophin http://purl.org/sig/ont/fma/fma62357
T3 137-143 Body_part denotes muscle http://purl.org/sig/ont/fma/fma32558

GlyCosmos600-MAT

Id Subject Object Predicate Lexical cue
PD-MAT-B_T1 137-143 http://purl.obolibrary.org/obo/MAT_0000025 denotes muscle

GlyCosmos600-GlycoProteins

Id Subject Object Predicate Lexical cue
PD-GlycoProteins-B_T5 66-76 https://acgg.asia/db/gpdb/id/GPDB0001626 denotes dystrophin
PD-GlycoProteins-B_T6 66-76 https://acgg.asia/db/gpdb/id/GPDB0001627 denotes dystrophin
PD-GlycoProteins-B_T7 66-76 https://acgg.asia/db/gpdb/id/GPDB0003351 denotes dystrophin

sentences

Id Subject Object Predicate Lexical cue
TextSentencer_T2 0-152 Sentence denotes Duchenne muscular dystrophy (DMD) is a genetic disorder caused by dystrophin mutations, characterized by chronic inflammation and severe muscle wasting.
T2 0-152 Sentence denotes Duchenne muscular dystrophy (DMD) is a genetic disorder caused by dystrophin mutations, characterized by chronic inflammation and severe muscle wasting.

pubmed-enju-pas

Id Subject Object Predicate Lexical cue
EnjuParser_T16 0-8 JJ denotes Duchenne
EnjuParser_T17 9-17 JJ denotes muscular
EnjuParser_T18 18-27 NN denotes dystrophy
EnjuParser_T19 28-29 -LRB- denotes (
EnjuParser_T20 29-32 NN denotes DMD
EnjuParser_T21 32-33 -RRB- denotes )
EnjuParser_T22 34-36 VBZ denotes is
EnjuParser_T23 37-38 DT denotes a
EnjuParser_T24 39-46 JJ denotes genetic
EnjuParser_T25 47-55 NN denotes disorder
EnjuParser_T26 56-62 VBN denotes caused
EnjuParser_T27 63-65 IN denotes by
EnjuParser_T28 66-76 NN denotes dystrophin
EnjuParser_T29 77-86 NNS denotes mutations
EnjuParser_T30 86-87 -COMMA- denotes ,
EnjuParser_T31 88-101 VBN denotes characterized
EnjuParser_T32 102-104 IN denotes by
EnjuParser_T33 105-112 JJ denotes chronic
EnjuParser_T34 113-125 NN denotes inflammation
EnjuParser_T35 126-129 CC denotes and
EnjuParser_T36 130-136 JJ denotes severe
EnjuParser_T37 137-143 NN denotes muscle
EnjuParser_T38 144-151 NN denotes wasting
EnjuParser_R15 EnjuParser_T18 EnjuParser_T16 arg1Of dystrophy,Duchenne
EnjuParser_R16 EnjuParser_T18 EnjuParser_T17 arg1Of dystrophy,muscular
EnjuParser_R17 EnjuParser_T18 EnjuParser_T19 arg1Of dystrophy,(
EnjuParser_R18 EnjuParser_T20 EnjuParser_T19 arg2Of DMD,(
EnjuParser_R19 EnjuParser_T21 EnjuParser_T19 arg3Of ),(
EnjuParser_R20 EnjuParser_T18 EnjuParser_T22 arg1Of dystrophy,is
EnjuParser_R21 EnjuParser_T25 EnjuParser_T22 arg2Of disorder,is
EnjuParser_R22 EnjuParser_T25 EnjuParser_T23 arg1Of disorder,a
EnjuParser_R23 EnjuParser_T25 EnjuParser_T24 arg1Of disorder,genetic
EnjuParser_R24 EnjuParser_T29 EnjuParser_T26 arg1Of mutations,caused
EnjuParser_R25 EnjuParser_T25 EnjuParser_T26 arg2Of disorder,caused
EnjuParser_R26 EnjuParser_T29 EnjuParser_T27 arg2Of mutations,by
EnjuParser_R27 EnjuParser_T29 EnjuParser_T28 arg1Of mutations,dystrophin
EnjuParser_R28 EnjuParser_T29 EnjuParser_T30 arg1Of mutations,","
EnjuParser_R29 EnjuParser_T35 EnjuParser_T31 arg1Of and,characterized
EnjuParser_R30 EnjuParser_T29 EnjuParser_T31 arg2Of mutations,characterized
EnjuParser_R31 EnjuParser_T35 EnjuParser_T32 arg2Of and,by
EnjuParser_R32 EnjuParser_T34 EnjuParser_T33 arg1Of inflammation,chronic
EnjuParser_R33 EnjuParser_T34 EnjuParser_T35 arg1Of inflammation,and
EnjuParser_R34 EnjuParser_T38 EnjuParser_T35 arg2Of wasting,and
EnjuParser_R35 EnjuParser_T38 EnjuParser_T36 arg1Of wasting,severe
EnjuParser_R36 EnjuParser_T38 EnjuParser_T37 arg1Of wasting,muscle

mondo_disease

Id Subject Object Predicate Lexical cue mondo_id
T1 0-27 Disease denotes Duchenne muscular dystrophy http://purl.obolibrary.org/obo/MONDO_0010679
T2 29-32 Disease denotes DMD http://purl.obolibrary.org/obo/MONDO_0010679
T3 39-55 Disease denotes genetic disorder http://purl.obolibrary.org/obo/MONDO_0003847
T4 113-125 Disease denotes inflammation http://purl.obolibrary.org/obo/MONDO_0021166
T5 137-151 Disease denotes muscle wasting http://purl.obolibrary.org/obo/MONDO_0004323

HP-phenotype

Id Subject Object Predicate Lexical cue hp_id
T1 9-27 Phenotype denotes muscular dystrophy HP:0003560
T2 137-151 Phenotype denotes muscle wasting HP:0003202

Anatomy-UBERON

Id Subject Object Predicate Lexical cue uberon_id
T2 137-143 Body_part denotes muscle http://purl.obolibrary.org/obo/UBERON_0001630|http://purl.obolibrary.org/obo/UBERON_0005090

Anatomy-MAT

Id Subject Object Predicate Lexical cue mat_id
T1 137-143 Body_part denotes muscle http://purl.obolibrary.org/obo/MAT_0000025