
PMC:7228307 / 41939-42656
Annnotations
LitCovid-PubTator
Id | Subject | Object | Predicate | Lexical cue | tao:has_database_id |
---|---|---|---|---|---|
714 | 225-233 | Gene | denotes | FcγRIIIa | Gene:2214 |
715 | 363-370 | Gene | denotes | FcγRIIb | Gene:2213 |
716 | 534-541 | Gene | denotes | FcγRIII | Gene:2214 |
717 | 577-585 | Gene | denotes | FcγRIIIa | Gene:2214 |
718 | 405-409 | Gene | denotes | FcγR | Gene:2213 |
719 | 206-210 | Gene | denotes | FcγR | Gene:2213 |
720 | 55-59 | Gene | denotes | FcγR | Gene:2213 |
721 | 645-652 | Species | denotes | patient | Tax:9606 |
722 | 292-297 | Disease | denotes | tumor | MESH:D009369 |
723 | 710-716 | Disease | denotes | cancer | MESH:D009369 |
LitCovid-PD-FMA-UBERON
Id | Subject | Object | Predicate | Lexical cue | fma_id |
---|---|---|---|---|---|
T359 | 298-303 | Body_part | denotes | cells | http://purl.org/sig/ont/fma/fma68646 |
LitCovid-PD-MONDO
Id | Subject | Object | Predicate | Lexical cue | mondo_id |
---|---|---|---|---|---|
T68 | 267-271 | Disease | denotes | ADCC | http://purl.obolibrary.org/obo/MONDO_0008734 |
T69 | 292-297 | Disease | denotes | tumor | http://purl.obolibrary.org/obo/MONDO_0005070 |
T70 | 710-716 | Disease | denotes | cancer | http://purl.obolibrary.org/obo/MONDO_0004992 |
LitCovid-PD-CLO
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T753 | 55-57 | http://purl.obolibrary.org/obo/CLO_0052676 | denotes | Fc |
T754 | 129-139 | http://purl.obolibrary.org/obo/CLO_0001658 | denotes | activation |
T755 | 190-200 | http://purl.obolibrary.org/obo/CLO_0001658 | denotes | activating |
T756 | 206-208 | http://purl.obolibrary.org/obo/CLO_0052676 | denotes | Fc |
T757 | 225-227 | http://purl.obolibrary.org/obo/CLO_0052676 | denotes | Fc |
T758 | 298-303 | http://purl.obolibrary.org/obo/GO_0005623 | denotes | cells |
T759 | 363-365 | http://purl.obolibrary.org/obo/CLO_0052676 | denotes | Fc |
T760 | 405-407 | http://purl.obolibrary.org/obo/CLO_0052676 | denotes | Fc |
T761 | 410-411 | http://purl.obolibrary.org/obo/CLO_0001020 | denotes | A |
T762 | 534-536 | http://purl.obolibrary.org/obo/CLO_0052676 | denotes | Fc |
T763 | 559-561 | http://purl.obolibrary.org/obo/CLO_0052676 | denotes | Fc |
T764 | 577-579 | http://purl.obolibrary.org/obo/CLO_0052676 | denotes | Fc |
LitCovid-PD-CHEBI
Id | Subject | Object | Predicate | Lexical cue | chebi_id |
---|---|---|---|---|---|
T218 | 60-68 | Chemical | denotes | effector | http://purl.obolibrary.org/obo/CHEBI_35224 |
LitCovid-sample-PD-IDO
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T212 | 298-303 | http://purl.obolibrary.org/obo/CL_0000000 | denotes | cells |
LitCovid-sample-Pubtator
Id | Subject | Object | Predicate | Lexical cue | pubann:denotes |
---|---|---|---|---|---|
714 | 225-233 | Gene | denotes | FcγRIIIa | Gene:2214 |
715 | 363-370 | Gene | denotes | FcγRIIb | Gene:2213 |
716 | 534-541 | Gene | denotes | FcγRIII | Gene:2214 |
717 | 577-585 | Gene | denotes | FcγRIIIa | Gene:2214 |
718 | 405-409 | Gene | denotes | FcγR | Gene:2213 |
719 | 206-210 | Gene | denotes | FcγR | Gene:2213 |
720 | 55-59 | Gene | denotes | FcγR | Gene:2213 |
721 | 645-652 | Species | denotes | patient | Tax:9606 |
722 | 292-297 | Disease | denotes | tumor | MESH:D009369 |
723 | 710-716 | Disease | denotes | cancer | MESH:D009369 |
LitCovid-sample-sentences
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T235 | 0-111 | Sentence | denotes | Thus, the challenge for the development of more potent FcγR effector mAbs is to overcome three major obstacles. |
T236 | 112-304 | Sentence | denotes | First, improving activation potency by selectively enhancing interaction with activating‐type FcγR, particularly FcγRIIIa owing to its predominant role in ADCC‐mediated killing of tumor cells. |
T237 | 305-371 | Sentence | denotes | Second, reducing binding interactions with the inhibitory FcγRIIb. |
T238 | 372-446 | Sentence | denotes | These two approaches improve the FcγR A‐to‐I ratio of cytotoxic IgG1 mAbs. |
T239 | 447-717 | Sentence | denotes | Third, overcoming the significant affinity difference in the interaction with the main FcγRIII allelic forms of FcγRIIIa‐V158 and FcγRIIIa‐F158 76, 83, 84 which appears to be an important source of patient variability in responses to therapeutic mAb treatment of cancer. |
LitCovid-sample-PD-FMA
Id | Subject | Object | Predicate | Lexical cue | fma_id |
---|---|---|---|---|---|
T358 | 298-303 | Body_part | denotes | cells | http://purl.org/sig/ont/fma/fma68646 |
LitCovid-sample-PD-GO-BP-0
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T106 | 267-271 | http://purl.obolibrary.org/obo/GO_0001788 | denotes | ADCC |
LitCovid-sample-PD-MONDO
Id | Subject | Object | Predicate | Lexical cue | mondo_id |
---|---|---|---|---|---|
T25 | 292-297 | Disease | denotes | tumor | http://purl.obolibrary.org/obo/MONDO_0005070 |
T26 | 710-716 | Disease | denotes | cancer | http://purl.obolibrary.org/obo/MONDO_0004992 |
LitCovid-sample-PD-HP
Id | Subject | Object | Predicate | Lexical cue | hp_id |
---|---|---|---|---|---|
T15 | 292-297 | Phenotype | denotes | tumor | http://purl.obolibrary.org/obo/HP_0002664 |
T16 | 710-716 | Phenotype | denotes | cancer | http://purl.obolibrary.org/obo/HP_0002664 |
LitCovid-sample-GO-BP
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T106 | 267-271 | http://purl.obolibrary.org/obo/GO_0001788 | denotes | ADCC |
LitCovid-PD-GO-BP
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T106 | 267-271 | http://purl.obolibrary.org/obo/GO_0001788 | denotes | ADCC |
LitCovid-sentences
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T235 | 0-111 | Sentence | denotes | Thus, the challenge for the development of more potent FcγR effector mAbs is to overcome three major obstacles. |
T236 | 112-304 | Sentence | denotes | First, improving activation potency by selectively enhancing interaction with activating‐type FcγR, particularly FcγRIIIa owing to its predominant role in ADCC‐mediated killing of tumor cells. |
T237 | 305-371 | Sentence | denotes | Second, reducing binding interactions with the inhibitory FcγRIIb. |
T238 | 372-446 | Sentence | denotes | These two approaches improve the FcγR A‐to‐I ratio of cytotoxic IgG1 mAbs. |
T239 | 447-717 | Sentence | denotes | Third, overcoming the significant affinity difference in the interaction with the main FcγRIII allelic forms of FcγRIIIa‐V158 and FcγRIIIa‐F158 76, 83, 84 which appears to be an important source of patient variability in responses to therapeutic mAb treatment of cancer. |
LitCovid-PD-HP
Id | Subject | Object | Predicate | Lexical cue | hp_id |
---|---|---|---|---|---|
T15 | 292-297 | Phenotype | denotes | tumor | http://purl.obolibrary.org/obo/HP_0002664 |
T16 | 710-716 | Phenotype | denotes | cancer | http://purl.obolibrary.org/obo/HP_0002664 |