PMC:7291971 / 13089-13274
Annnotations
LitCovid-PMC-OGER-BB
{"project":"LitCovid-PMC-OGER-BB","denotations":[{"id":"T304","span":{"begin":14,"end":39},"obj":"CHEBI:86228;CHEBI:86228"},{"id":"T305","span":{"begin":109,"end":124},"obj":"GO:0006306"},{"id":"T306","span":{"begin":170,"end":179},"obj":"CHEBI:22260;CHEBI:22260"}],"text":"Recently, the 2-nitrobenzenesulfonamide has been used successfully to synthetize transition state analogs of DNA methylation based on the coupling of cytosine analogs to adenosine [15]."}
LitCovid-PD-FMA-UBERON
{"project":"LitCovid-PD-FMA-UBERON","denotations":[{"id":"T52","span":{"begin":109,"end":112},"obj":"Body_part"},{"id":"T53","span":{"begin":150,"end":158},"obj":"Body_part"}],"attributes":[{"id":"A52","pred":"fma_id","subj":"T52","obj":"http://purl.org/sig/ont/fma/fma74412"},{"id":"A53","pred":"fma_id","subj":"T53","obj":"http://purl.org/sig/ont/fma/fma82776"}],"text":"Recently, the 2-nitrobenzenesulfonamide has been used successfully to synthetize transition state analogs of DNA methylation based on the coupling of cytosine analogs to adenosine [15]."}
LitCovid-PubTator
{"project":"LitCovid-PubTator","denotations":[{"id":"240","span":{"begin":14,"end":39},"obj":"Chemical"},{"id":"241","span":{"begin":150,"end":158},"obj":"Chemical"},{"id":"242","span":{"begin":170,"end":179},"obj":"Chemical"}],"attributes":[{"id":"A241","pred":"tao:has_database_id","subj":"241","obj":"MESH:D003596"},{"id":"A242","pred":"tao:has_database_id","subj":"242","obj":"MESH:D000241"}],"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":"Recently, the 2-nitrobenzenesulfonamide has been used successfully to synthetize transition state analogs of DNA methylation based on the coupling of cytosine analogs to adenosine [15]."}
LitCovid-PD-CLO
{"project":"LitCovid-PD-CLO","denotations":[{"id":"T119","span":{"begin":40,"end":43},"obj":"http://purl.obolibrary.org/obo/CLO_0051582"}],"text":"Recently, the 2-nitrobenzenesulfonamide has been used successfully to synthetize transition state analogs of DNA methylation based on the coupling of cytosine analogs to adenosine [15]."}
LitCovid-PD-CHEBI
{"project":"LitCovid-PD-CHEBI","denotations":[{"id":"T219","span":{"begin":109,"end":112},"obj":"Chemical"},{"id":"T220","span":{"begin":150,"end":158},"obj":"Chemical"},{"id":"T221","span":{"begin":170,"end":179},"obj":"Chemical"}],"attributes":[{"id":"A219","pred":"chebi_id","subj":"T219","obj":"http://purl.obolibrary.org/obo/CHEBI_16991"},{"id":"A220","pred":"chebi_id","subj":"T220","obj":"http://purl.obolibrary.org/obo/CHEBI_16040"},{"id":"A221","pred":"chebi_id","subj":"T221","obj":"http://purl.obolibrary.org/obo/CHEBI_16335"}],"text":"Recently, the 2-nitrobenzenesulfonamide has been used successfully to synthetize transition state analogs of DNA methylation based on the coupling of cytosine analogs to adenosine [15]."}
LitCovid-PD-GO-BP
{"project":"LitCovid-PD-GO-BP","denotations":[{"id":"T30","span":{"begin":109,"end":124},"obj":"http://purl.obolibrary.org/obo/GO_0006306"},{"id":"T31","span":{"begin":113,"end":124},"obj":"http://purl.obolibrary.org/obo/GO_0032259"}],"text":"Recently, the 2-nitrobenzenesulfonamide has been used successfully to synthetize transition state analogs of DNA methylation based on the coupling of cytosine analogs to adenosine [15]."}
LitCovid-sentences
{"project":"LitCovid-sentences","denotations":[{"id":"T80","span":{"begin":0,"end":185},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"Recently, the 2-nitrobenzenesulfonamide has been used successfully to synthetize transition state analogs of DNA methylation based on the coupling of cytosine analogs to adenosine [15]."}