PubMed:20106987 / 121-295 JSONTXT

{"project":"sentences","denotations":[{"id":"T2","span":{"begin":0,"end":174},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"Ullrich congenital muscular dystrophy (UCMD) is a disabling and life-threatening disorder resulting from either recessive or dominant mutations in genes encoding collagen VI."}

{"project":"PubmedHPO","denotations":[{"id":"T1","span":{"begin":8,"end":37},"obj":"HP_0003741"},{"id":"T2","span":{"begin":19,"end":37},"obj":"HP_0003560"}],"text":"Ullrich congenital muscular dystrophy (UCMD) is a disabling and life-threatening disorder resulting from either recessive or dominant mutations in genes encoding collagen VI."}

{"project":"Allie","denotations":[{"id":"SS1_20106987_1_0","span":{"begin":0,"end":37},"obj":"expanded"},{"id":"SS2_20106987_1_0","span":{"begin":39,"end":43},"obj":"abbr"}],"relations":[{"id":"AE1_20106987_1_0","pred":"abbreviatedTo","subj":"SS1_20106987_1_0","obj":"SS2_20106987_1_0"}],"text":"Ullrich congenital muscular dystrophy (UCMD) is a disabling and life-threatening disorder resulting from either recessive or dominant mutations in genes encoding collagen VI."}

{"project":"PubCasesHPO","denotations":[{"id":"AB1","span":{"begin":8,"end":37},"obj":"HP:0003741"}],"text":"Ullrich congenital muscular dystrophy (UCMD) is a disabling and life-threatening disorder resulting from either recessive or dominant mutations in genes encoding collagen VI."}

{"project":"mondo_disease","denotations":[{"id":"T3","span":{"begin":0,"end":37},"obj":"Disease"},{"id":"T5","span":{"begin":39,"end":43},"obj":"Disease"}],"attributes":[{"id":"A3","pred":"mondo_id","subj":"T3","obj":"http://purl.obolibrary.org/obo/MONDO_0000355"},{"id":"A4","pred":"mondo_id","subj":"T3","obj":"http://purl.obolibrary.org/obo/MONDO_0009681"},{"id":"A5","pred":"mondo_id","subj":"T5","obj":"http://purl.obolibrary.org/obo/MONDO_0000355"}],"text":"Ullrich congenital muscular dystrophy (UCMD) is a disabling and life-threatening disorder resulting from either recessive or dominant mutations in genes encoding collagen VI."}

{"project":"HP-phenotype","denotations":[{"id":"T2","span":{"begin":8,"end":37},"obj":"Phenotype"}],"attributes":[{"id":"A2","pred":"hp_id","subj":"T2","obj":"HP:0003560"}],"namespaces":[{"prefix":"HP","uri":"http://purl.obolibrary.org/obo/HP_"}],"text":"Ullrich congenital muscular dystrophy (UCMD) is a disabling and life-threatening disorder resulting from either recessive or dominant mutations in genes encoding collagen VI."}