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PubMed:15958417 / 209-319 JSONTXT

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sentences

Id Subject Object Predicate Lexical cue
TextSentencer_T3 0-110 Sentence denotes Mutations in the human homolog (LARGE) have been described in a form of congenital muscular dystrophy (MDC1D).
T3 0-110 Sentence denotes Mutations in the human homolog (LARGE) have been described in a form of congenital muscular dystrophy (MDC1D).

GlycoBiology-GDGDB

Id Subject Object Predicate Lexical cue
_T2 32-37 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00383 denotes LARGE
_T11 72-101 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00381 denotes congenital muscular dystrophy
_T12 72-108 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00383 denotes congenital muscular dystrophy (MDC1D
_T13 103-108 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00383 denotes MDC1D

ICD10

Id Subject Object Predicate Lexical cue
T1 83-101 http://purl.bioontology.org/ontology/ICD10/G71.0 denotes muscular dystrophy

uniprot-human

Id Subject Object Predicate Lexical cue
T2 32-37 http://www.uniprot.org/uniprot/Q9UH22 denotes LARGE

HP-phenotype

Id Subject Object Predicate Lexical cue hp_id
T1 72-101 Phenotype denotes congenital muscular dystrophy HP:0003560

mondo_disease

Id Subject Object Predicate Lexical cue mondo_id
T2 72-101 Disease denotes congenital muscular dystrophy http://purl.obolibrary.org/obo/MONDO_0019950
T3 103-108 Disease denotes MDC1D http://purl.obolibrary.org/obo/MONDO_0012138

NCBITAXON

Id Subject Object Predicate Lexical cue db_id
T3 17-22 OrganismTaxon denotes human 9606