PMC:7755033 / 754-1120 JSONTXT

{"project":"LitCovid-PubTator","denotations":[{"id":"29","span":{"begin":10,"end":14},"obj":"Gene"},{"id":"30","span":{"begin":313,"end":317},"obj":"Gene"},{"id":"32","span":{"begin":351,"end":356},"obj":"Gene"},{"id":"37","span":{"begin":4,"end":9},"obj":"Species"},{"id":"38","span":{"begin":307,"end":312},"obj":"Species"},{"id":"39","span":{"begin":328,"end":331},"obj":"Species"},{"id":"40","span":{"begin":332,"end":335},"obj":"Species"},{"id":"41","span":{"begin":340,"end":350},"obj":"Species"},{"id":"47","span":{"begin":258,"end":260},"obj":"Species"}],"attributes":[{"id":"A29","pred":"tao:has_database_id","subj":"29","obj":"Gene:59272"},{"id":"A30","pred":"tao:has_database_id","subj":"30","obj":"Gene:59272"},{"id":"A32","pred":"tao:has_database_id","subj":"32","obj":"Gene:43740568"},{"id":"A37","pred":"tao:has_database_id","subj":"37","obj":"Tax:9606"},{"id":"A38","pred":"tao:has_database_id","subj":"38","obj":"Tax:9606"},{"id":"A39","pred":"tao:has_database_id","subj":"39","obj":"Tax:2698737"},{"id":"A40","pred":"tao:has_database_id","subj":"40","obj":"Tax:11118"},{"id":"A41","pred":"tao:has_database_id","subj":"41","obj":"Tax:2697049"},{"id":"A47","pred":"tao:has_database_id","subj":"47","obj":"Tax:126910"}],"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":"and human ACE2 receptor using in silico methods. Most of the phytoconstituents displayed good absorption and transport kinetics and were also found to display no associated mutagenic or adverse effect(s). Molecular docking analyses revealed that most of the WS phytoconstituents exhibited potent binding to human ACE2 receptor, SAR-CoV and SARS-CoV-2 spike glycoprot"}

{"project":"LitCovid-sentences","denotations":[{"id":"T11","span":{"begin":49,"end":204},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"and human ACE2 receptor using in silico methods. Most of the phytoconstituents displayed good absorption and transport kinetics and were also found to display no associated mutagenic or adverse effect(s). Molecular docking analyses revealed that most of the WS phytoconstituents exhibited potent binding to human ACE2 receptor, SAR-CoV and SARS-CoV-2 spike glycoprot"}