PMC:7571312 / 10227-10619
Annnotations
LitCovid-PD-CLO
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T8217 | 244-245 | http://purl.obolibrary.org/obo/CLO_0001020 | denotes | a |
| T52201 | 286-287 | http://purl.obolibrary.org/obo/CLO_0001020 | denotes | a |
| T96491 | 330-331 | http://purl.obolibrary.org/obo/CLO_0001020 | denotes | a |
LitCovid-PD-CHEBI
| Id | Subject | Object | Predicate | Lexical cue | chebi_id |
|---|---|---|---|---|---|
| T123 | 37-43 | Chemical | denotes | ketone | http://purl.obolibrary.org/obo/CHEBI_17087 |
LitCovid-sentences
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T51 | 0-173 | Sentence | denotes | Central to our strategy of examining ketone-based thiophiles was the preparation of an array of intermediates containing diverse methylketone moieties and protecting groups. |
| T52 | 174-392 | Sentence | denotes | The preparation of halomethylketone intermediates was accomplished in a two-step procedure by the generation of a diazoketone intermediate31 or directly by a modified Kowalski–Haque reaction,32 as depicted in Scheme 1. |
LitCovid-PubTator
| Id | Subject | Object | Predicate | Lexical cue | tao:has_database_id |
|---|---|---|---|---|---|
| 258 | 37-43 | Chemical | denotes | ketone | MESH:D007659 |
| 259 | 129-141 | Chemical | denotes | methylketone | MESH:D000096 |
| 260 | 193-209 | Chemical | denotes | halomethylketone | |
| 261 | 288-299 | Chemical | denotes | diazoketone |
2_test
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| 33054210-1433192-61913455 | 312-314 | 1433192 | denotes | 31 |
| 33054210-10746010-61913456 | 365-367 | 10746010 | denotes | 32 |