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PubMed:20106987 / 58-87 JSONTXT

Annnotations TAB JSON ListView MergeView

PubCasesHPO

Id Subject Object Predicate Lexical cue
TI1 0-29 HP:0003741 denotes congenital muscular dystrophy

HP-phenotype

Id Subject Object Predicate Lexical cue hp_id
T1 0-29 Phenotype denotes congenital muscular dystrophy HP:0003560