CORD-19:775b90287b44353bee979abb0970a4666022f86d / 612168-612292 JSONTXT

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    CORD-19-Sentences

    {"project":"CORD-19-Sentences","denotations":[{"id":"T8804","span":{"begin":0,"end":124},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"Previous cases of siblings with AR-CGD have shown variable phenotype, presumably due to penetrance of the functional allele."}

    CORD-19_Custom_license_subset

    {"project":"CORD-19_Custom_license_subset","denotations":[{"id":"T225","span":{"begin":0,"end":124},"obj":"Sentence"}],"text":"Previous cases of siblings with AR-CGD have shown variable phenotype, presumably due to penetrance of the functional allele."}

    CORD-19-PD-MONDO

    {"project":"CORD-19-PD-MONDO","denotations":[{"id":"T4713","span":{"begin":32,"end":34},"obj":"Disease"},{"id":"T4714","span":{"begin":35,"end":38},"obj":"Disease"},{"id":"T56697","span":{"begin":32,"end":34},"obj":"Disease"},{"id":"T47610","span":{"begin":35,"end":38},"obj":"Disease"}],"attributes":[{"id":"A4713","pred":"mondo_id","subj":"T4713","obj":"http://purl.obolibrary.org/obo/MONDO_0011786"},{"id":"A4714","pred":"mondo_id","subj":"T4714","obj":"http://purl.obolibrary.org/obo/MONDO_0010600"},{"id":"A4715","pred":"mondo_id","subj":"T4714","obj":"http://purl.obolibrary.org/obo/MONDO_0018305"},{"id":"A34942","pred":"mondo_id","subj":"T56697","obj":"http://purl.obolibrary.org/obo/MONDO_0011786"},{"id":"A7850","pred":"mondo_id","subj":"T47610","obj":"http://purl.obolibrary.org/obo/MONDO_0010600"},{"id":"A99030","pred":"mondo_id","subj":"T47610","obj":"http://purl.obolibrary.org/obo/MONDO_0018305"}],"text":"Previous cases of siblings with AR-CGD have shown variable phenotype, presumably due to penetrance of the functional allele."}

    CORD-19-PD-HP

    {"project":"CORD-19-PD-HP","denotations":[{"id":"T3345","span":{"begin":32,"end":34},"obj":"Phenotype"}],"attributes":[{"id":"A3345","pred":"hp_id","subj":"T3345","obj":"http://purl.obolibrary.org/obo/HP_0003193"}],"text":"Previous cases of siblings with AR-CGD have shown variable phenotype, presumably due to penetrance of the functional allele."}