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PMC:7291971 / 12778-12974 JSONTXT

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LitCovid-PMC-OGER-BB

Id Subject Object Predicate Lexical cue
T300 40-54 CHEBI:32877;CHEBI:32877 denotes primary amines
T301 81-105 CHEBI:53325;CHEBI:53325 denotes nitrobenzenesulfonamides
T302 110-116 CHEBI:32988;CHEBI:32988 denotes amides
T303 154-159 CHEBI:24433;CHEBI:24433 denotes group

LitCovid-PubTator

Id Subject Object Predicate Lexical cue tao:has_database_id
237 48-54 Chemical denotes amines MESH:D000588
238 81-105 Chemical denotes nitrobenzenesulfonamides
239 107-116 Chemical denotes Ns-amides

LitCovid-PD-MONDO

Id Subject Object Predicate Lexical cue mondo_id
T33 107-109 Disease denotes Ns http://purl.obolibrary.org/obo/MONDO_0009735

LitCovid-PD-CLO

Id Subject Object Predicate Lexical cue
T114 56-57 http://purl.obolibrary.org/obo/CLO_0001020 denotes a
T115 126-127 http://purl.obolibrary.org/obo/CLO_0001020 denotes a
T116 143-153 http://purl.obolibrary.org/obo/CLO_0001658 denotes activating
T117 160-163 http://purl.obolibrary.org/obo/CLO_0051582 denotes has
T118 192-194 http://purl.obolibrary.org/obo/CLO_0050507 denotes 22

LitCovid-PD-CHEBI

Id Subject Object Predicate Lexical cue chebi_id
T213 40-54 Chemical denotes primary amines http://purl.obolibrary.org/obo/CHEBI_32877
T214 48-54 Chemical denotes amines http://purl.obolibrary.org/obo/CHEBI_32952
T215 107-109 Chemical denotes Ns http://purl.obolibrary.org/obo/CHEBI_33349|http://purl.obolibrary.org/obo/CHEBI_33355
T217 110-116 Chemical denotes amides http://purl.obolibrary.org/obo/CHEBI_32988
T218 154-159 Chemical denotes group http://purl.obolibrary.org/obo/CHEBI_24433

LitCovid-sentences

Id Subject Object Predicate Lexical cue
T78 0-196 Sentence denotes To circumvent the lack of reactivity of primary amines, a synthetic method using nitrobenzenesulfonamides (Ns-amides) as both a protecting and activating group has been developed by Fukuyama [22].