CORD-19:775b90287b44353bee979abb0970a4666022f86d / 139184-139390 JSONTXT

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    CORD-19-Sentences

    {"project":"CORD-19-Sentences","denotations":[{"id":"T62967","span":{"begin":0,"end":206},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"Morquio A Syndrome (also known as mucopolysaccharidase type IVA deficiency) is an autosomal-recessive lysosomal storage disease characterized by a deficiency of the N-acetylgalactosamine-6 sulfatase enzyme."}

    CORD-19_Custom_license_subset

    {"project":"CORD-19_Custom_license_subset","denotations":[{"id":"T2","span":{"begin":0,"end":206},"obj":"Sentence"}],"text":"Morquio A Syndrome (also known as mucopolysaccharidase type IVA deficiency) is an autosomal-recessive lysosomal storage disease characterized by a deficiency of the N-acetylgalactosamine-6 sulfatase enzyme."}

    CORD-19-PD-MONDO

    {"project":"CORD-19-PD-MONDO","denotations":[{"id":"T909","span":{"begin":60,"end":63},"obj":"Disease"},{"id":"T910","span":{"begin":102,"end":127},"obj":"Disease"},{"id":"T35898","span":{"begin":60,"end":63},"obj":"Disease"},{"id":"T14128","span":{"begin":102,"end":127},"obj":"Disease"}],"attributes":[{"id":"A909","pred":"mondo_id","subj":"T909","obj":"http://purl.obolibrary.org/obo/MONDO_0009475"},{"id":"A910","pred":"mondo_id","subj":"T910","obj":"http://purl.obolibrary.org/obo/MONDO_0002561"},{"id":"A57729","pred":"mondo_id","subj":"T35898","obj":"http://purl.obolibrary.org/obo/MONDO_0009475"},{"id":"A61105","pred":"mondo_id","subj":"T14128","obj":"http://purl.obolibrary.org/obo/MONDO_0002561"}],"text":"Morquio A Syndrome (also known as mucopolysaccharidase type IVA deficiency) is an autosomal-recessive lysosomal storage disease characterized by a deficiency of the N-acetylgalactosamine-6 sulfatase enzyme."}