> top > docs > PubMed:20106987 > spans > 50-87 > annotations

PubMed:20106987 / 50-87 JSONTXT

Annnotations TAB JSON ListView MergeView

DisGeNET

Id Subject Object Predicate Lexical cue
T1 0-37 disease:C0410179 denotes Ullrich congenital muscular dystrophy

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
20106987-0#50#87#diseaseC0410179 0-37 diseaseC0410179 denotes Ullrich congenital muscular dystrophy

PubCasesHPO

Id Subject Object Predicate Lexical cue
TI1 8-37 HP:0003741 denotes congenital muscular dystrophy

mondo_disease

Id Subject Object Predicate Lexical cue mondo_id
T1 0-37 Disease denotes Ullrich congenital muscular dystrophy http://purl.obolibrary.org/obo/MONDO_0000355|http://purl.obolibrary.org/obo/MONDO_0009681

HP-phenotype

Id Subject Object Predicate Lexical cue hp_id
T1 8-37 Phenotype denotes congenital muscular dystrophy HP:0003560