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PubMed:25533456 / 0-268 JSONTXT

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sentences

Id Subject Object Predicate Lexical cue
TextSentencer_T1 0-141 Sentence denotes Aberrant mitochondria in a Bethlem myopathy patient with a homozygous amino acid substitution that destabilizes the collagen VI α2(VI) chain.
T1 0-141 Sentence denotes Aberrant mitochondria in a Bethlem myopathy patient with a homozygous amino acid substitution that destabilizes the collagen VI α2(VI) chain.

PubmedHPO

Id Subject Object Predicate Lexical cue
T1 150-158 HP_0003198 denotes myopathy
T2 171-200 HP_0003741 denotes congenital muscular dystrophy
T3 182-200 HP_0003560 denotes muscular dystrophy

PubCasesHPO

Id Subject Object Predicate Lexical cue
AB1 152-160 HP:0003198 denotes opathy a
AB2 173-202 HP:0003741 denotes ngenital muscular dystrophy (

PubCasesORDO

Id Subject Object Predicate Lexical cue
AB1 142-158 ORDO:610 denotes Bethlem myopathy
TI1 27-43 ORDO:610 denotes Bethlem myopathy

HP-phenotype

Id Subject Object Predicate Lexical cue hp_id
T1 35-43 Phenotype denotes myopathy HP:0003198
T2 150-158 Phenotype denotes myopathy HP:0003198
T3 171-200 Phenotype denotes congenital muscular dystrophy HP:0003560

mondo_disease

Id Subject Object Predicate Lexical cue mondo_id
T1 27-43 Disease denotes Bethlem myopathy http://purl.obolibrary.org/obo/MONDO_0008029|http://purl.obolibrary.org/obo/MONDO_0024530
T3 142-158 Disease denotes Bethlem myopathy http://purl.obolibrary.org/obo/MONDO_0008029|http://purl.obolibrary.org/obo/MONDO_0024530
T5 163-200 Disease denotes Ullrich congenital muscular dystrophy http://purl.obolibrary.org/obo/MONDO_0000355|http://purl.obolibrary.org/obo/MONDO_0009681
T7 202-206 Disease denotes UCMD http://purl.obolibrary.org/obo/MONDO_0000355

NCBITAXON

Id Subject Object Predicate Lexical cue db_id
T1 44-51 OrganismTaxon denotes patient 9606