PMC:7291971 / 12778-12974
Annnotations
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]. |