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PubMed:22453924 / 0-169 JSONTXT

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sentences

Id Subject Object Predicate Lexical cue
TextSentencer_T1 0-131 Sentence denotes Novel mutation in spectrin-like repeat 1 of dystrophin central domain causes protein misfolding and mild Becker muscular dystrophy.
T1 0-131 Sentence denotes Novel mutation in spectrin-like repeat 1 of dystrophin central domain causes protein misfolding and mild Becker muscular dystrophy.

DisGeNET

Id Subject Object Predicate Lexical cue
T0 44-54 gene:1756 denotes dystrophin
T1 105-130 disease:C0917713 denotes Becker muscular dystrophy
T2 149-159 gene:1756 denotes dystrophin
R1 T0 T1 associated_with dystrophin,Becker muscular dystrophy

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
22453924-0#44#54#gene1756 44-54 gene1756 denotes dystrophin
22453924-0#105#130#diseaseC0917713 105-130 diseaseC0917713 denotes Becker muscular dystrophy
44#54#gene1756105#130#diseaseC0917713 22453924-0#44#54#gene1756 22453924-0#105#130#diseaseC0917713 associated_with dystrophin,Becker muscular dystrophy

UBERON-AE

Id Subject Object Predicate Lexical cue
PD-UBERON-AE-B_T1 55-62 http://purl.obolibrary.org/obo/UBERON_0012131 denotes central

PubCasesHPO

Id Subject Object Predicate Lexical cue
TI1 112-130 HP:0003560 denotes muscular dystrophy

performance-test

Id Subject Object Predicate Lexical cue
PD-UBERON-AE-B_T2 55-62 http://purl.obolibrary.org/obo/UBERON_0012131 denotes central

PubCasesORDO

Id Subject Object Predicate Lexical cue
TI1 105-130 ORDO:98895 denotes Becker muscular dystrophy

mondo_disease

Id Subject Object Predicate Lexical cue mondo_id
T1 105-130 Disease denotes Becker muscular dystrophy http://purl.obolibrary.org/obo/MONDO_0010311

HP-phenotype

Id Subject Object Predicate Lexical cue hp_id
T1 112-130 Phenotype denotes muscular dystrophy HP:0003560