PubMed:22337883
Annnotations
sentences
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 0-119 | Sentence | denotes | The transcription factor Erg controls endothelial cell quiescence by repressing activity of nuclear factor (NF)-κB p65. |
T2 | 120-244 | Sentence | denotes | The interaction of transcription factors with specific DNA sequences is critical for activation of gene expression programs. |
T3 | 245-436 | Sentence | denotes | In endothelial cells (EC), the transcription factor NF-κB is important in the switch from quiescence to activation, and is tightly controlled to avoid excessive inflammation and organ damage. |
T4 | 437-516 | Sentence | denotes | Here we describe a novel mechanism that controls the activation of NF-κB in EC. |
T5 | 517-665 | Sentence | denotes | The transcription factor Erg, the most highly expressed ETS member in resting EC, controls quiescence by repressing proinflammatory gene expression. |
T6 | 666-850 | Sentence | denotes | Focusing on intercellular adhesion molecule 1(ICAM)-1 as a model, we identify two ETS binding sites (EBS -118 and -181) within the ICAM-1 promoter required for Erg-mediated repression. |
T7 | 851-954 | Sentence | denotes | We show that Erg binds to both EBS -118 and EBS -181, the latter located within the NF-κB binding site. |
T8 | 955-1122 | Sentence | denotes | Interestingly, inhibition of Erg expression in quiescent EC results in increased NF-κB-dependent ICAM-1 expression, indicating that Erg represses basal NF-κB activity. |
T9 | 1123-1229 | Sentence | denotes | Erg prevents NF-κB p65 from binding to the ICAM-1 promoter, suggesting a direct mechanism of interference. |
T10 | 1230-1475 | Sentence | denotes | Gene set enrichment analysis of transcriptome profiles of Erg and NF-κB-dependent genes, together with chromatin immunoprecipitation (ChIP) studies, reveals that this mechanism is common to other proinflammatory genes, including cIAP-2 and IL-8. |
T11 | 1476-1657 | Sentence | denotes | These results identify a role for Erg as a gatekeeper controlling vascular inflammation, thus providing an important barrier to protect against inappropriate endothelial activation. |
Inflammaging
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 0-119 | Sentence | denotes | The transcription factor Erg controls endothelial cell quiescence by repressing activity of nuclear factor (NF)-κB p65. |
T2 | 120-244 | Sentence | denotes | The interaction of transcription factors with specific DNA sequences is critical for activation of gene expression programs. |
T3 | 245-436 | Sentence | denotes | In endothelial cells (EC), the transcription factor NF-κB is important in the switch from quiescence to activation, and is tightly controlled to avoid excessive inflammation and organ damage. |
T4 | 437-516 | Sentence | denotes | Here we describe a novel mechanism that controls the activation of NF-κB in EC. |
T5 | 517-665 | Sentence | denotes | The transcription factor Erg, the most highly expressed ETS member in resting EC, controls quiescence by repressing proinflammatory gene expression. |
T6 | 666-850 | Sentence | denotes | Focusing on intercellular adhesion molecule 1(ICAM)-1 as a model, we identify two ETS binding sites (EBS -118 and -181) within the ICAM-1 promoter required for Erg-mediated repression. |
T7 | 851-954 | Sentence | denotes | We show that Erg binds to both EBS -118 and EBS -181, the latter located within the NF-κB binding site. |
T8 | 955-1122 | Sentence | denotes | Interestingly, inhibition of Erg expression in quiescent EC results in increased NF-κB-dependent ICAM-1 expression, indicating that Erg represses basal NF-κB activity. |
T9 | 1123-1229 | Sentence | denotes | Erg prevents NF-κB p65 from binding to the ICAM-1 promoter, suggesting a direct mechanism of interference. |
T10 | 1230-1475 | Sentence | denotes | Gene set enrichment analysis of transcriptome profiles of Erg and NF-κB-dependent genes, together with chromatin immunoprecipitation (ChIP) studies, reveals that this mechanism is common to other proinflammatory genes, including cIAP-2 and IL-8. |
T11 | 1476-1657 | Sentence | denotes | These results identify a role for Erg as a gatekeeper controlling vascular inflammation, thus providing an important barrier to protect against inappropriate endothelial activation. |
T1 | 0-119 | Sentence | denotes | The transcription factor Erg controls endothelial cell quiescence by repressing activity of nuclear factor (NF)-κB p65. |
T2 | 120-244 | Sentence | denotes | The interaction of transcription factors with specific DNA sequences is critical for activation of gene expression programs. |
T3 | 245-436 | Sentence | denotes | In endothelial cells (EC), the transcription factor NF-κB is important in the switch from quiescence to activation, and is tightly controlled to avoid excessive inflammation and organ damage. |
T4 | 437-516 | Sentence | denotes | Here we describe a novel mechanism that controls the activation of NF-κB in EC. |
T5 | 517-665 | Sentence | denotes | The transcription factor Erg, the most highly expressed ETS member in resting EC, controls quiescence by repressing proinflammatory gene expression. |
T6 | 666-850 | Sentence | denotes | Focusing on intercellular adhesion molecule 1(ICAM)-1 as a model, we identify two ETS binding sites (EBS -118 and -181) within the ICAM-1 promoter required for Erg-mediated repression. |
T7 | 851-954 | Sentence | denotes | We show that Erg binds to both EBS -118 and EBS -181, the latter located within the NF-κB binding site. |
T8 | 955-1122 | Sentence | denotes | Interestingly, inhibition of Erg expression in quiescent EC results in increased NF-κB-dependent ICAM-1 expression, indicating that Erg represses basal NF-κB activity. |
T9 | 1123-1229 | Sentence | denotes | Erg prevents NF-κB p65 from binding to the ICAM-1 promoter, suggesting a direct mechanism of interference. |
T10 | 1230-1475 | Sentence | denotes | Gene set enrichment analysis of transcriptome profiles of Erg and NF-κB-dependent genes, together with chromatin immunoprecipitation (ChIP) studies, reveals that this mechanism is common to other proinflammatory genes, including cIAP-2 and IL-8. |
T11 | 1476-1657 | Sentence | denotes | These results identify a role for Erg as a gatekeeper controlling vascular inflammation, thus providing an important barrier to protect against inappropriate endothelial activation. |
bionlp-st-pc-2013-training
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 25-28 | Gene_or_gene_product | denotes | Erg |
T2 | 92-114 | Complex | denotes | nuclear factor (NF)-κB |
T3 | 115-118 | Gene_or_gene_product | denotes | p65 |
T4 | 297-302 | Complex | denotes | NF-κB |
T5 | 504-509 | Complex | denotes | NF-κB |
T6 | 542-545 | Gene_or_gene_product | denotes | Erg |
T7 | 573-576 | Gene_or_gene_product | denotes | ETS |
T8 | 678-719 | Gene_or_gene_product | denotes | intercellular adhesion molecule 1(ICAM)-1 |
T9 | 748-751 | Gene_or_gene_product | denotes | ETS |
T10 | 797-803 | Gene_or_gene_product | denotes | ICAM-1 |
T11 | 826-829 | Gene_or_gene_product | denotes | Erg |
T12 | 864-867 | Gene_or_gene_product | denotes | Erg |
T13 | 935-940 | Complex | denotes | NF-κB |
T14 | 984-987 | Gene_or_gene_product | denotes | Erg |
T15 | 1036-1041 | Complex | denotes | NF-κB |
T16 | 1052-1058 | Gene_or_gene_product | denotes | ICAM-1 |
T17 | 1087-1090 | Gene_or_gene_product | denotes | Erg |
T18 | 1107-1112 | Complex | denotes | NF-κB |
T19 | 1123-1126 | Gene_or_gene_product | denotes | Erg |
T20 | 1136-1141 | Complex | denotes | NF-κB |
T21 | 1142-1145 | Gene_or_gene_product | denotes | p65 |
T22 | 1166-1172 | Gene_or_gene_product | denotes | ICAM-1 |
T23 | 1288-1291 | Gene_or_gene_product | denotes | Erg |
T24 | 1296-1301 | Complex | denotes | NF-κB |
T25 | 1333-1342 | Cellular_component | denotes | chromatin |
T26 | 1459-1465 | Gene_or_gene_product | denotes | cIAP-2 |
T27 | 1470-1474 | Gene_or_gene_product | denotes | IL-8 |
T28 | 1510-1513 | Gene_or_gene_product | denotes | Erg |
Allie
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
SS1_22337883_0_0 | 92-106 | expanded | denotes | nuclear factor |
SS2_22337883_0_0 | 108-110 | abbr | denotes | NF |
SS1_22337883_2_0 | 248-265 | expanded | denotes | endothelial cells |
SS2_22337883_2_0 | 267-269 | abbr | denotes | EC |
SS1_22337883_9_0 | 1333-1362 | expanded | denotes | chromatin immunoprecipitation |
SS2_22337883_9_0 | 1364-1368 | abbr | denotes | ChIP |
AE1_22337883_0_0 | SS1_22337883_0_0 | SS2_22337883_0_0 | abbreviatedTo | nuclear factor,NF |
AE1_22337883_2_0 | SS1_22337883_2_0 | SS2_22337883_2_0 | abbreviatedTo | endothelial cells,EC |
AE1_22337883_9_0 | SS1_22337883_9_0 | SS2_22337883_9_0 | abbreviatedTo | chromatin immunoprecipitation,ChIP |
mondo_disease
Id | Subject | Object | Predicate | Lexical cue | mondo_id |
---|---|---|---|---|---|
T1 | 406-418 | Disease | denotes | inflammation | http://purl.obolibrary.org/obo/MONDO_0021166 |
T2 | 767-770 | Disease | denotes | EBS | http://purl.obolibrary.org/obo/MONDO_0017610 |
T3 | 882-885 | Disease | denotes | EBS | http://purl.obolibrary.org/obo/MONDO_0017610 |
T4 | 895-898 | Disease | denotes | EBS | http://purl.obolibrary.org/obo/MONDO_0017610 |
T5 | 1551-1563 | Disease | denotes | inflammation | http://purl.obolibrary.org/obo/MONDO_0021166 |
NCBITAXON
Id | Subject | Object | Predicate | Lexical cue | db_id |
---|---|---|---|---|---|
T1 | 1519-1529 | OrganismTaxon | denotes | gatekeeper | 2795565 |
Anatomy-UBERON
Id | Subject | Object | Predicate | Lexical cue | uberon_id |
---|---|---|---|---|---|
T1 | 38-54 | Body_part | denotes | endothelial cell | http://purl.obolibrary.org/obo/CL_0000115 |
T2 | 248-265 | Body_part | denotes | endothelial cells | http://purl.obolibrary.org/obo/CL_0000115 |
T3 | 267-269 | Body_part | denotes | EC | http://purl.obolibrary.org/obo/CL_0000115 |
T4 | 423-428 | Body_part | denotes | organ | http://purl.obolibrary.org/obo/UBERON_0000062|http://purl.obolibrary.org/obo/UBERON_0003103 |
T6 | 513-515 | Body_part | denotes | EC | http://purl.obolibrary.org/obo/CL_0000115 |
T7 | 595-597 | Body_part | denotes | EC | http://purl.obolibrary.org/obo/CL_0000115 |
T8 | 1012-1014 | Body_part | denotes | EC | http://purl.obolibrary.org/obo/CL_0000115 |
CL-cell
Id | Subject | Object | Predicate | Lexical cue | cl_id |
---|---|---|---|---|---|
T1 | 38-54 | Cell | denotes | endothelial cell | http://purl.obolibrary.org/obo/CL:0000115 |
T2 | 248-265 | Cell | denotes | endothelial cells | http://purl.obolibrary.org/obo/CL:0000115 |
T3 | 267-269 | Cell | denotes | EC | http://purl.obolibrary.org/obo/CL:0000115 |
T4 | 513-515 | Cell | denotes | EC | http://purl.obolibrary.org/obo/CL:0000115 |
T5 | 595-597 | Cell | denotes | EC | http://purl.obolibrary.org/obo/CL:0000115 |
T6 | 1012-1014 | Cell | denotes | EC | http://purl.obolibrary.org/obo/CL:0000115 |
T7 | 1101-1106 | Cell | denotes | basal | http://purl.obolibrary.org/obo/CL:0002324 |