CORD-19:f212d6366a45726107a30bde1f4615c28cb5ce22 / 88813-89068 JSONTXT

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    CORD-19_Custom_license_subset

    {"project":"CORD-19_Custom_license_subset","denotations":[{"id":"T183","span":{"begin":0,"end":255},"obj":"Sentence"}],"text":"244 Polyglutamine diseases are a specific group of hereditary neurodegeneration caused by expansion of CAG triplet repeats in an exon of disease genes which leads to the production of a disease protein containing an expanded polyglutamine, polyQ, stretch."}

    CORD-19-Sentences

    {"project":"CORD-19-Sentences","denotations":[{"id":"T62746","span":{"begin":0,"end":255},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"244 Polyglutamine diseases are a specific group of hereditary neurodegeneration caused by expansion of CAG triplet repeats in an exon of disease genes which leads to the production of a disease protein containing an expanded polyglutamine, polyQ, stretch."}

    CORD-19-PD-HP

    {"project":"CORD-19-PD-HP","denotations":[{"id":"T8","span":{"begin":62,"end":79},"obj":"Phenotype"}],"attributes":[{"id":"A8","pred":"hp_id","subj":"T8","obj":"http://purl.obolibrary.org/obo/HP_0002180"}],"text":"244 Polyglutamine diseases are a specific group of hereditary neurodegeneration caused by expansion of CAG triplet repeats in an exon of disease genes which leads to the production of a disease protein containing an expanded polyglutamine, polyQ, stretch."}