PMC:7696151 / 3994-4302 JSONTXT

{"project":"LitCovid-PubTator","denotations":[{"id":"116","span":{"begin":178,"end":206},"obj":"Chemical"},{"id":"118","span":{"begin":219,"end":227},"obj":"Disease"}],"attributes":[{"id":"A118","pred":"tao:has_database_id","subj":"118","obj":"MESH:D064420"}],"namespaces":[{"prefix":"Tax","uri":"https://www.ncbi.nlm.nih.gov/taxonomy/"},{"prefix":"MESH","uri":"https://id.nlm.nih.gov/mesh/"},{"prefix":"Gene","uri":"https://www.ncbi.nlm.nih.gov/gene/"},{"prefix":"CVCL","uri":"https://web.expasy.org/cellosaurus/CVCL_"}],"text":"ed the stereoselective processes in the metabolism of the molecule [9].\nStudies of structure-activity relationships have demonstrated that the halogen substitutions of different 4-aminoquinolinesderivatives reduced the toxicity, but it also reduced the pharmacological activity. Instead, the therapeutic rati"}

{"project":"LitCovid-sentences","denotations":[{"id":"T33","span":{"begin":72,"end":278},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"ed the stereoselective processes in the metabolism of the molecule [9].\nStudies of structure-activity relationships have demonstrated that the halogen substitutions of different 4-aminoquinolinesderivatives reduced the toxicity, but it also reduced the pharmacological activity. Instead, the therapeutic rati"}