CORD-19:2008f024274c53b0de1276f4047a6a641813fd98 / 118027-118147 JSONTXT

{"project":"CORD-19-Sentences","denotations":[{"id":"T45690","span":{"begin":0,"end":120},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"Introduction-C1-esterase inhibitor (C1-INH) deficiency is a rare disorder classified into acquired and hereditary forms."}

{"project":"Epistemic_Statements","denotations":[{"id":"T209","span":{"begin":0,"end":120},"obj":"Epistemic_statement"}],"text":"Introduction-C1-esterase inhibitor (C1-INH) deficiency is a rare disorder classified into acquired and hereditary forms."}

{"project":"CORD-19_Custom_license_subset","denotations":[{"id":"T203","span":{"begin":0,"end":120},"obj":"Sentence"}],"text":"Introduction-C1-esterase inhibitor (C1-INH) deficiency is a rare disorder classified into acquired and hereditary forms."}