PubMed:21054465
Annnotations
LitCoin-entities
| Id | Subject | Object | Predicate | Lexical cue | db_id |
|---|---|---|---|---|---|
| 8261 | 23-29 | GeneOrGeneProduct | denotes | CYP2C8 | NCBIGene:1558 |
| 8262 | 33-45 | DiseaseOrPhenotypicFeature | denotes | hypertensive | MESH:D006973 |
| 8263 | 46-54 | OrganismTaxon | denotes | patients | NCBITaxon:9606 |
| 8264 | 141-147 | GeneOrGeneProduct | denotes | CYP2C8 | NCBIGene:1558 |
| 8265 | 167-200 | GeneOrGeneProduct | denotes | cytochrome P450 (CYP) epoxygenase | NCBIGene:1558 |
| 8266 | 210-226 | ChemicalEntity | denotes | Arachidonic acid | MESH:D016718 |
| 8267 | 247-274 | ChemicalEntity | denotes | epoxyeicosatrienenoic acids | |
| 8268 | 279-307 | ChemicalEntity | denotes | hydroxyeicosatetrenoic acids | |
| 8269 | 337-349 | DiseaseOrPhenotypicFeature | denotes | hypertension | MESH:D006973 |
| 8270 | 451-457 | GeneOrGeneProduct | denotes | CYP2C8 | NCBIGene:1558 |
| 8271 | 563-575 | DiseaseOrPhenotypicFeature | denotes | hypertensive | MESH:D006973 |
| 8272 | 576-584 | OrganismTaxon | denotes | patients | NCBITaxon:9606 |
| 8273 | 633-639 | GeneOrGeneProduct | denotes | CYP2C8 | NCBIGene:1558 |
| 8274 | 690-696 | GeneOrGeneProduct | denotes | CYP2C8 | NCBIGene:1558 |
| 8275 | 730-738 | OrganismTaxon | denotes | patients | NCBITaxon:9606 |
| 8276 | 744-756 | DiseaseOrPhenotypicFeature | denotes | hypertension | MESH:D006973 |
| 8277 | 842-860 | SequenceVariant | denotes | T deletion at 5063 | c|DEL|5063|T |
| 8278 | 881-896 | SequenceVariant | denotes | C to T at 33468 | c|SUB|C|33468|T |
| 8279 | 982-994 | DiseaseOrPhenotypicFeature | denotes | hypertensive | MESH:D006973 |
| 8280 | 995-1003 | OrganismTaxon | denotes | patients | NCBITaxon:9606 |
| 8281 | 1058-1065 | SequenceVariant | denotes | C35322C | c|SUB|C|35322|C |
| 8282 | 1082-1090 | OrganismTaxon | denotes | patients | NCBITaxon:9606 |
| 8283 | 1182-1189 | SequenceVariant | denotes | C35322C | c|SUB|C|35322|C |
| 8284 | 1223-1235 | DiseaseOrPhenotypicFeature | denotes | hypertension | MESH:D006973 |
| 8285 | 1411-1418 | SequenceVariant | denotes | C35322T | c|SUB|C|35322|T |
| 8286 | 1442-1454 | DiseaseOrPhenotypicFeature | denotes | hypertensive | MESH:D006973 |
| 8287 | 1455-1463 | OrganismTaxon | denotes | patients | NCBITaxon:9606 |
LitCoin-sentences
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 0-111 | Sentence | denotes | Mutational analysis of CYP2C8 in hypertensive patients using denaturing high performance liquid chromatography. |
| T2 | 112-209 | Sentence | denotes | WHAT IS KNOWN AND OBJECTIVE: CYP2C8 is involved in the cytochrome P450 (CYP) epoxygenase pathway. |
| T3 | 210-350 | Sentence | denotes | Arachidonic acid metabolites such as epoxyeicosatrienenoic acids and hydroxyeicosatetrenoic acids, produced may have a role in hypertension. |
| T4 | 351-522 | Sentence | denotes | We aimed to develop a medium through-put method for screening samples of known and new mutations of CYP2C8 using denaturing high performance liquid chromatography (DHPLC). |
| T5 | 523-652 | Sentence | denotes | METHODS: DNA samples from 200 subjects (hypertensive patients and healthy controls) were screened for SNPs in CYP2C8 using DHPLC. |
| T6 | 653-771 | Sentence | denotes | Genotypes and allelic frequencies of CYP2C8 between the healthy controls and patients with hypertension were compared. |
| T7 | 772-796 | Sentence | denotes | RESULTS AND DISCUSSIONS: |
| T8 | 797-907 | Sentence | denotes | Six variants were detected and two were new; T deletion at 5063 and substitution of C to T at 33468 in exon 8. |
| T9 | 908-1004 | Sentence | denotes | Differences in variant frequencies were detected between the controls and hypertensive patients. |
| T10 | 1005-1091 | Sentence | denotes | The controls have significantly higher prevalence of C35322C compared to the patients. |
| T11 | 1092-1163 | Sentence | denotes | The functional significance of the SNP at 35322 requires further study. |
| T12 | 1164-1236 | Sentence | denotes | Having homozygous C35322C could be a protective factor for hypertension. |
| T13 | 1237-1264 | Sentence | denotes | WHAT IS NEW AND CONCLUSION: |
| T14 | 1265-1384 | Sentence | denotes | Denaturing high performance liquid chromatography is useful for population screening to identify new and existing SNPs. |
| T15 | 1385-1486 | Sentence | denotes | A higher frequency of the C35322T SNP was observed among hypertensive patients than control subjects. |
| T16 | 1487-1587 | Sentence | denotes | This potentially important observation requires confirmation and the clinical significance assessed. |
LitCoin-SeqVar
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 1058-1065 | SequenceVariant | denotes | C35322C |
| T2 | 1182-1189 | SequenceVariant | denotes | C35322C |
| T3 | 1411-1418 | SequenceVariant | denotes | C35322T |
LitCoin-GeneOrGeneProduct-v0
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 0-10 | GeneOrGeneProduct | denotes | Mutational |
| T2 | 23-29 | GeneOrGeneProduct | denotes | CYP2C8 |
| T3 | 33-45 | GeneOrGeneProduct | denotes | hypertensive |
| T4 | 72-76 | GeneOrGeneProduct | denotes | high |
| T5 | 141-147 | GeneOrGeneProduct | denotes | CYP2C8 |
| T6 | 167-182 | GeneOrGeneProduct | denotes | cytochrome P450 |
| T7 | 184-187 | GeneOrGeneProduct | denotes | CYP |
| T8 | 222-226 | GeneOrGeneProduct | denotes | acid |
| T9 | 269-278 | GeneOrGeneProduct | denotes | acids and |
| T10 | 302-307 | GeneOrGeneProduct | denotes | acids |
| T11 | 337-349 | GeneOrGeneProduct | denotes | hypertension |
| T12 | 392-398 | GeneOrGeneProduct | denotes | method |
| T13 | 438-447 | GeneOrGeneProduct | denotes | mutations |
| T14 | 451-457 | GeneOrGeneProduct | denotes | CYP2C8 |
| T15 | 475-479 | GeneOrGeneProduct | denotes | high |
| T16 | 523-530 | GeneOrGeneProduct | denotes | METHODS |
| T17 | 563-575 | GeneOrGeneProduct | denotes | hypertensive |
| T18 | 633-639 | GeneOrGeneProduct | denotes | CYP2C8 |
| T19 | 675-686 | GeneOrGeneProduct | denotes | frequencies |
| T20 | 690-696 | GeneOrGeneProduct | denotes | CYP2C8 |
| T21 | 744-756 | GeneOrGeneProduct | denotes | hypertension |
| T22 | 931-942 | GeneOrGeneProduct | denotes | frequencies |
| T23 | 982-994 | GeneOrGeneProduct | denotes | hypertensive |
| T24 | 1212-1218 | GeneOrGeneProduct | denotes | factor |
| T25 | 1223-1235 | GeneOrGeneProduct | denotes | hypertension |
| T26 | 1276-1280 | GeneOrGeneProduct | denotes | high |
| T27 | 1394-1403 | GeneOrGeneProduct | denotes | frequency |
| T28 | 1442-1454 | GeneOrGeneProduct | denotes | hypertensive |
LitCoin-GeneOrGeneProduct-v2
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 23-29 | GeneOrGeneProduct | denotes | CYP2C8 |
| T2 | 72-76 | GeneOrGeneProduct | denotes | high |
| T3 | 141-147 | GeneOrGeneProduct | denotes | CYP2C8 |
| T4 | 167-182 | GeneOrGeneProduct | denotes | cytochrome P450 |
| T5 | 184-187 | GeneOrGeneProduct | denotes | CYP |
| T6 | 222-226 | GeneOrGeneProduct | denotes | acid |
| T7 | 337-349 | GeneOrGeneProduct | denotes | hypertension |
| T8 | 392-398 | GeneOrGeneProduct | denotes | method |
| T9 | 451-457 | GeneOrGeneProduct | denotes | CYP2C8 |
| T10 | 475-479 | GeneOrGeneProduct | denotes | high |
| T11 | 633-639 | GeneOrGeneProduct | denotes | CYP2C8 |
| T12 | 690-696 | GeneOrGeneProduct | denotes | CYP2C8 |
| T13 | 744-756 | GeneOrGeneProduct | denotes | hypertension |
| T14 | 1212-1218 | GeneOrGeneProduct | denotes | factor |
| T15 | 1223-1235 | GeneOrGeneProduct | denotes | hypertension |
| T16 | 1276-1280 | GeneOrGeneProduct | denotes | high |
| T17 | 1394-1403 | GeneOrGeneProduct | denotes | frequency |
LitCoin-Disease-MeSH
| Id | Subject | Object | Predicate | Lexical cue | originalLabel |
|---|---|---|---|---|---|
| T1 | 33-45 | DiseaseOrPhenotypicFeature | denotes | hypertensive | D006973 |
| T2 | 337-349 | DiseaseOrPhenotypicFeature | denotes | hypertension | D006973 |
| T3 | 563-575 | DiseaseOrPhenotypicFeature | denotes | hypertensive | D006973 |
| T4 | 744-756 | DiseaseOrPhenotypicFeature | denotes | hypertension | D006973 |
| T5 | 982-994 | DiseaseOrPhenotypicFeature | denotes | hypertensive | D006973 |
| T6 | 1223-1235 | DiseaseOrPhenotypicFeature | denotes | hypertension | D006973 |
| T7 | 1442-1454 | DiseaseOrPhenotypicFeature | denotes | hypertensive | D006973 |
LitCoin-GeneOrGeneProduct-v3
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 23-29 | GeneOrGeneProduct | denotes | CYP2C8 |
| T2 | 141-147 | GeneOrGeneProduct | denotes | CYP2C8 |
| T3 | 167-182 | GeneOrGeneProduct | denotes | cytochrome P450 |
| T4 | 184-187 | GeneOrGeneProduct | denotes | CYP |
| T5 | 451-457 | GeneOrGeneProduct | denotes | CYP2C8 |
| T6 | 633-639 | GeneOrGeneProduct | denotes | CYP2C8 |
| T7 | 690-696 | GeneOrGeneProduct | denotes | CYP2C8 |
LitCoin_Mondo_095
| Id | Subject | Object | Predicate | Lexical cue | mondo_id |
|---|---|---|---|---|---|
| T1 | 337-349 | DiseaseOrPhenotypicFeature | denotes | hypertension | 0005044 |
| T2 | 744-756 | DiseaseOrPhenotypicFeature | denotes | hypertension | 0005044 |
| T3 | 1223-1235 | DiseaseOrPhenotypicFeature | denotes | hypertension | 0005044 |
LitCoin-MeSH-Disease-2
| Id | Subject | Object | Predicate | Lexical cue | ID: |
|---|---|---|---|---|---|
| T1 | 337-349 | DiseaseOrPhenotypicFeature | denotes | hypertension | D006973 |
| T2 | 744-756 | DiseaseOrPhenotypicFeature | denotes | hypertension | D006973 |
| T3 | 1223-1235 | DiseaseOrPhenotypicFeature | denotes | hypertension | D006973 |
LitCoin-MONDO_bioort2019
| Id | Subject | Object | Predicate | Lexical cue | #label |
|---|---|---|---|---|---|
| T1 | 337-349 | DiseaseOrPhenotypicFeature | denotes | hypertension | D006973 |
| T2 | 744-756 | DiseaseOrPhenotypicFeature | denotes | hypertension | D006973 |
| T3 | 1223-1235 | DiseaseOrPhenotypicFeature | denotes | hypertension | D006973 |
LitCoin-Chemical-MeSH-CHEBI
| Id | Subject | Object | Predicate | Lexical cue | ID: |
|---|---|---|---|---|---|
| T1 | 167-182 | ChemicalEntity | denotes | cytochrome P450 | http://purl.obolibrary.org/obo/CHEBI_38559 |
| T2 | 184-187 | ChemicalEntity | denotes | CYP | http://purl.obolibrary.org/obo/CHEBI_38559 |
| T3 | 210-226 | ChemicalEntity | denotes | Arachidonic acid | http://purl.obolibrary.org/obo/CHEBI_15843 |
| T4 | 247-274 | ChemicalEntity | denotes | epoxyeicosatrienenoic acids | ChemicalEntity |
| T5 | 279-307 | ChemicalEntity | denotes | hydroxyeicosatetrenoic acids | ChemicalEntity |
LitCoin-NCBITaxon-2
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 46-54 | OrganismTaxon | denotes | patients |
| T2 | 576-584 | OrganismTaxon | denotes | patients |
| T3 | 730-738 | OrganismTaxon | denotes | patients |
| T4 | 995-1003 | OrganismTaxon | denotes | patients |
| T5 | 1082-1090 | OrganismTaxon | denotes | patients |
| T6 | 1455-1463 | OrganismTaxon | denotes | patients |
LitCoin-training-merged
| Id | Subject | Object | Predicate | Lexical cue | #label | ID: |
|---|---|---|---|---|---|---|
| T5 | 279-307 | ChemicalEntity | denotes | hydroxyeicosatetrenoic acids | ChemicalEntity | |
| T4 | 247-274 | ChemicalEntity | denotes | epoxyeicosatrienenoic acids | ChemicalEntity | |
| T3 | 210-226 | ChemicalEntity | denotes | Arachidonic acid | http://purl.obolibrary.org/obo/CHEBI_15843 | |
| T2 | 184-187 | ChemicalEntity | denotes | CYP | http://purl.obolibrary.org/obo/CHEBI_38559 | |
| T1 | 167-182 | ChemicalEntity | denotes | cytochrome P450 | http://purl.obolibrary.org/obo/CHEBI_38559 | |
| T7 | 690-696 | GeneOrGeneProduct | denotes | CYP2C8 | ||
| T6 | 633-639 | GeneOrGeneProduct | denotes | CYP2C8 | ||
| T1312 | 451-457 | GeneOrGeneProduct | denotes | CYP2C8 | ||
| T65247 | 184-187 | GeneOrGeneProduct | denotes | CYP | ||
| T13678 | 167-182 | GeneOrGeneProduct | denotes | cytochrome P450 | ||
| T53383 | 141-147 | GeneOrGeneProduct | denotes | CYP2C8 | ||
| T60092 | 23-29 | GeneOrGeneProduct | denotes | CYP2C8 | ||
| T25414 | 1223-1235 | DiseaseOrPhenotypicFeature | denotes | hypertension | D006973 | |
| T9810 | 744-756 | DiseaseOrPhenotypicFeature | denotes | hypertension | D006973 | |
| T6284 | 337-349 | DiseaseOrPhenotypicFeature | denotes | hypertension | D006973 | |
| T5414 | 1455-1463 | OrganismTaxon | denotes | patients | ||
| T46354 | 1082-1090 | OrganismTaxon | denotes | patients | ||
| T16600 | 995-1003 | OrganismTaxon | denotes | patients | ||
| T97472 | 730-738 | OrganismTaxon | denotes | patients | ||
| T27071 | 576-584 | OrganismTaxon | denotes | patients | ||
| T32716 | 46-54 | OrganismTaxon | denotes | patients | ||
| T33311 | 1411-1418 | SequenceVariant | denotes | C35322T | ||
| T6930 | 1182-1189 | SequenceVariant | denotes | C35322C | ||
| T80582 | 1058-1065 | SequenceVariant | denotes | C35322C |
DisGeNET
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T0 | 690-696 | gene:1558 | denotes | CYP2C8 |
| T1 | 744-756 | disease:C0020538 | denotes | hypertension |
| R1 | T0 | T1 | associated_with | CYP2C8,hypertension |
Allie
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| SS1_21054465_4_0 | 464-513 | expanded | denotes | denaturing high performance liquid chromatography |
| SS2_21054465_4_0 | 515-520 | abbr | denotes | DHPLC |
| AE1_21054465_4_0 | SS1_21054465_4_0 | SS2_21054465_4_0 | abbreviatedTo | denaturing high performance liquid chromatography,DHPLC |
PubmedHPO
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 337-349 | HP_0000822 | denotes | hypertension |
biored-valid
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 23-29 | GeneOrGeneProduct | denotes | CYP2C8 |
| T2 | 33-45 | DiseaseOrPhenotypicFeature | denotes | hypertensive |
| T3 | 46-54 | OrganismTaxon | denotes | patients |
| T4 | 141-147 | GeneOrGeneProduct | denotes | CYP2C8 |
| T5 | 167-200 | GeneOrGeneProduct | denotes | cytochrome P450 (CYP) epoxygenase |
| T6 | 210-226 | ChemicalEntity | denotes | Arachidonic acid |
| T7 | 247-274 | ChemicalEntity | denotes | epoxyeicosatrienenoic acids |
| T8 | 279-307 | ChemicalEntity | denotes | hydroxyeicosatetrenoic acids |
| T9 | 337-349 | DiseaseOrPhenotypicFeature | denotes | hypertension |
| T10 | 451-457 | GeneOrGeneProduct | denotes | CYP2C8 |
| T11 | 563-575 | DiseaseOrPhenotypicFeature | denotes | hypertensive |
| T12 | 576-584 | OrganismTaxon | denotes | patients |
| T13 | 633-639 | GeneOrGeneProduct | denotes | CYP2C8 |
| T14 | 690-696 | GeneOrGeneProduct | denotes | CYP2C8 |
| T15 | 730-738 | OrganismTaxon | denotes | patients |
| T16 | 744-756 | DiseaseOrPhenotypicFeature | denotes | hypertension |
| T17 | 842-860 | SequenceVariant | denotes | T deletion at 5063 |
| T18 | 881-896 | SequenceVariant | denotes | C to T at 33468 |
| T19 | 982-994 | DiseaseOrPhenotypicFeature | denotes | hypertensive |
| T20 | 995-1003 | OrganismTaxon | denotes | patients |
| T21 | 1058-1065 | SequenceVariant | denotes | C35322C |
| T22 | 1082-1090 | OrganismTaxon | denotes | patients |
| T23 | 1182-1189 | SequenceVariant | denotes | C35322C |
| T24 | 1223-1235 | DiseaseOrPhenotypicFeature | denotes | hypertension |
| T25 | 1411-1418 | SequenceVariant | denotes | C35322T |
| T26 | 1442-1454 | DiseaseOrPhenotypicFeature | denotes | hypertensive |
| T27 | 1455-1463 | OrganismTaxon | denotes | patients |
biored-valid-deepseek-nr-ng
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 0-10 | SequenceVariant | denotes | Mutational |
| T2 | 23-29 | GeneOrGeneProduct | denotes | CYP2C8 |
| T3 | 46-54 | DiseaseOrPhenotypicFeature | denotes | patients |
| T4 | 141-147 | GeneOrGeneProduct | denotes | CYP2C8 |
| T5 | 337-349 | DiseaseOrPhenotypicFeature | denotes | hypertension |
| T6 | 438-447 | SequenceVariant | denotes | mutations |
| T7 | 451-457 | GeneOrGeneProduct | denotes | CYP2C8 |
| T8 | 525-526 | SequenceVariant | denotes | T |
| T9 | 576-584 | DiseaseOrPhenotypicFeature | denotes | patients |
| T10 | 625-629 | SequenceVariant | denotes | SNPs |
| T11 | 744-756 | DiseaseOrPhenotypicFeature | denotes | hypertension |
| T12 | 801-809 | SequenceVariant | denotes | variants |
| T13 | 844-852 | SequenceVariant | denotes | deletion |
| T14 | 900-906 | SequenceVariant | denotes | exon 8 |
| T15 | 995-1003 | DiseaseOrPhenotypicFeature | denotes | patients |
| T16 | 1058-1065 | SequenceVariant | denotes | C35322C |
| T17 | 1411-1418 | SequenceVariant | denotes | C35322T |
biored-valid-deepseek-nr-g
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 23-29 | GeneOrGeneProduct | denotes | CYP2C8 |
| T2 | 33-54 | DiseaseOrPhenotypicFeature | denotes | hypertensive patients |
| T3 | 141-147 | GeneOrGeneProduct | denotes | CYP2C8 |
| T4 | 167-182 | GeneOrGeneProduct | denotes | cytochrome P450 |
| T5 | 210-226 | ChemicalEntity | denotes | Arachidonic acid |
| T6 | 337-349 | DiseaseOrPhenotypicFeature | denotes | hypertension |
| T7 | 451-457 | GeneOrGeneProduct | denotes | CYP2C8 |
| T8 | 515-520 | ChemicalEntity | denotes | DHPLC |
| T9 | 532-535 | ChemicalEntity | denotes | DNA |
| T10 | 563-584 | DiseaseOrPhenotypicFeature | denotes | hypertensive patients |
| T11 | 625-629 | SequenceVariant | denotes | SNPs |
| T12 | 633-639 | GeneOrGeneProduct | denotes | CYP2C8 |
| T13 | 646-651 | ChemicalEntity | denotes | DHPLC |
| T14 | 744-756 | DiseaseOrPhenotypicFeature | denotes | hypertension |
| T15 | 801-808 | SequenceVariant | denotes | variant |
| T16 | 1058-1065 | SequenceVariant | denotes | C35322C |
| T17 | 1127-1130 | SequenceVariant | denotes | SNP |
| T18 | 1223-1235 | DiseaseOrPhenotypicFeature | denotes | hypertension |
| T19 | 1411-1418 | SequenceVariant | denotes | C35322T |
biored-valid-deepseek-r-ng
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 23-29 | GeneOrGeneProduct | denotes | CYP2C8 |
| T2 | 33-54 | DiseaseOrPhenotypicFeature | denotes | hypertensive patients |
| T3 | 210-226 | ChemicalEntity | denotes | Arachidonic acid |
| T4 | 247-274 | ChemicalEntity | denotes | epoxyeicosatrienenoic acids |
| T5 | 279-307 | ChemicalEntity | denotes | hydroxyeicosatetrenoic acids |
| T6 | 337-349 | DiseaseOrPhenotypicFeature | denotes | hypertension |
| T7 | 625-629 | SequenceVariant | denotes | SNPs |
| T8 | 842-860 | SequenceVariant | denotes | T deletion at 5063 |
| T9 | 865-906 | SequenceVariant | denotes | substitution of C to T at 33468 in exon 8 |
| T10 | 1058-1065 | SequenceVariant | denotes | C35322C |
| T11 | 1127-1139 | SequenceVariant | denotes | SNP at 35322 |
| T12 | 1411-1422 | SequenceVariant | denotes | C35322T SNP |
biored-valid-deepseek-r-g
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 23-29 | GeneOrGeneProduct | denotes | CYP2C8 |
| T2 | 33-45 | DiseaseOrPhenotypicFeature | denotes | hypertensive |
| T3 | 141-147 | GeneOrGeneProduct | denotes | CYP2C8 |
| T4 | 167-182 | GeneOrGeneProduct | denotes | cytochrome P450 |
| T5 | 210-226 | ChemicalEntity | denotes | Arachidonic acid |
| T6 | 247-274 | ChemicalEntity | denotes | epoxyeicosatrienenoic acids |
| T7 | 279-307 | ChemicalEntity | denotes | hydroxyeicosatetrenoic acids |
| T8 | 337-349 | DiseaseOrPhenotypicFeature | denotes | hypertension |
| T9 | 438-447 | SequenceVariant | denotes | mutations |
| T10 | 451-457 | GeneOrGeneProduct | denotes | CYP2C8 |
| T11 | 563-575 | DiseaseOrPhenotypicFeature | denotes | hypertensive |
| T12 | 625-629 | SequenceVariant | denotes | SNPs |
| T13 | 633-639 | GeneOrGeneProduct | denotes | CYP2C8 |
| T14 | 690-696 | GeneOrGeneProduct | denotes | CYP2C8 |
| T15 | 744-756 | DiseaseOrPhenotypicFeature | denotes | hypertension |
| T16 | 801-809 | SequenceVariant | denotes | variants |
| T17 | 842-852 | SequenceVariant | denotes | T deletion |
| T18 | 865-887 | SequenceVariant | denotes | substitution of C to T |
| T19 | 982-994 | DiseaseOrPhenotypicFeature | denotes | hypertensive |
| T20 | 1058-1065 | SequenceVariant | denotes | C35322C |
| T21 | 1127-1139 | SequenceVariant | denotes | SNP at 35322 |
| T22 | 1171-1189 | SequenceVariant | denotes | homozygous C35322C |
| T23 | 1223-1235 | DiseaseOrPhenotypicFeature | denotes | hypertension |
| T24 | 1379-1383 | SequenceVariant | denotes | SNPs |
| T25 | 1411-1422 | SequenceVariant | denotes | C35322T SNP |
| T26 | 1442-1454 | DiseaseOrPhenotypicFeature | denotes | hypertensive |
biored-valid-gemini-nr-ng
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 23-29 | GeneOrGeneProduct | denotes | CYP2C8 |
| T2 | 33-45 | DiseaseOrPhenotypicFeature | denotes | hypertensive |
| T3 | 141-147 | GeneOrGeneProduct | denotes | CYP2C8 |
| T4 | 167-182 | GeneOrGeneProduct | denotes | cytochrome P450 |
| T5 | 210-226 | ChemicalEntity | denotes | Arachidonic acid |
| T6 | 247-274 | ChemicalEntity | denotes | epoxyeicosatrienenoic acids |
| T7 | 279-307 | ChemicalEntity | denotes | hydroxyeicosatetrenoic acids |
| T8 | 337-349 | DiseaseOrPhenotypicFeature | denotes | hypertension |
| T9 | 451-457 | GeneOrGeneProduct | denotes | CYP2C8 |
| T10 | 532-535 | ChemicalEntity | denotes | DNA |
| T11 | 563-575 | DiseaseOrPhenotypicFeature | denotes | hypertensive |
| T12 | 625-629 | SequenceVariant | denotes | SNPs |
| T13 | 633-639 | GeneOrGeneProduct | denotes | CYP2C8 |
| T14 | 744-756 | DiseaseOrPhenotypicFeature | denotes | hypertension |
| T15 | 777-778 | ChemicalEntity | denotes | T |
| T16 | 787-788 | ChemicalEntity | denotes | C |
| T17 | 842-843 | ChemicalEntity | denotes | T |
| T18 | 856-860 | SequenceVariant | denotes | 5063 |
| T19 | 891-896 | SequenceVariant | denotes | 33468 |
| T20 | 982-994 | DiseaseOrPhenotypicFeature | denotes | hypertensive |
| T21 | 1058-1065 | SequenceVariant | denotes | C35322C |
| T22 | 1127-1130 | SequenceVariant | denotes | SNP |
| T23 | 1223-1235 | DiseaseOrPhenotypicFeature | denotes | hypertension |
| T24 | 1379-1383 | SequenceVariant | denotes | SNPs |
| T25 | 1411-1418 | SequenceVariant | denotes | C35322T |
| T26 | 1442-1454 | DiseaseOrPhenotypicFeature | denotes | hypertensive |
biored-valid-gemini-r-ng
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 23-29 | GeneOrGeneProduct | denotes | CYP2C8 |
| T2 | 33-45 | DiseaseOrPhenotypicFeature | denotes | hypertensive |
| T3 | 61-110 | ChemicalEntity | denotes | denaturing high performance liquid chromatography |
| T4 | 141-147 | GeneOrGeneProduct | denotes | CYP2C8 |
| T5 | 167-182 | GeneOrGeneProduct | denotes | cytochrome P450 |
| T6 | 210-226 | ChemicalEntity | denotes | Arachidonic acid |
| T7 | 247-274 | ChemicalEntity | denotes | epoxyeicosatrienenoic acids |
| T8 | 279-307 | ChemicalEntity | denotes | hydroxyeicosatetrenoic acids |
| T9 | 337-349 | DiseaseOrPhenotypicFeature | denotes | hypertension |
| T10 | 451-457 | GeneOrGeneProduct | denotes | CYP2C8 |
| T11 | 464-513 | ChemicalEntity | denotes | denaturing high performance liquid chromatography |
| T12 | 515-520 | ChemicalEntity | denotes | DHPLC |
| T13 | 532-535 | ChemicalEntity | denotes | DNA |
| T14 | 563-575 | DiseaseOrPhenotypicFeature | denotes | hypertensive |
| T15 | 625-629 | SequenceVariant | denotes | SNPs |
| T16 | 633-639 | GeneOrGeneProduct | denotes | CYP2C8 |
| T17 | 646-651 | ChemicalEntity | denotes | DHPLC |
| T18 | 744-756 | DiseaseOrPhenotypicFeature | denotes | hypertension |
| T19 | 842-860 | SequenceVariant | denotes | T deletion at 5063 |
| T20 | 865-896 | SequenceVariant | denotes | substitution of C to T at 33468 |
| T21 | 982-994 | DiseaseOrPhenotypicFeature | denotes | hypertensive |
| T22 | 1058-1065 | SequenceVariant | denotes | C35322C |
| T23 | 1127-1139 | SequenceVariant | denotes | SNP at 35322 |
| T24 | 1171-1189 | SequenceVariant | denotes | homozygous C35322C |
| T25 | 1223-1235 | DiseaseOrPhenotypicFeature | denotes | hypertension |
| T26 | 1265-1314 | ChemicalEntity | denotes | Denaturing high performance liquid chromatography |
| T27 | 1379-1383 | SequenceVariant | denotes | SNPs |
| T28 | 1411-1422 | SequenceVariant | denotes | C35322T SNP |
| T29 | 1442-1454 | DiseaseOrPhenotypicFeature | denotes | hypertensive |
biored-valid-gemini-r-g
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 23-29 | GeneOrGeneProduct | denotes | CYP2C8 |
| T2 | 33-45 | DiseaseOrPhenotypicFeature | denotes | hypertensive |
| T3 | 141-147 | GeneOrGeneProduct | denotes | CYP2C8 |
| T4 | 167-182 | GeneOrGeneProduct | denotes | cytochrome P450 |
| T5 | 210-226 | ChemicalEntity | denotes | Arachidonic acid |
| T6 | 247-274 | ChemicalEntity | denotes | epoxyeicosatrienenoic acids |
| T7 | 279-307 | ChemicalEntity | denotes | hydroxyeicosatetrenoic acids |
| T8 | 337-349 | DiseaseOrPhenotypicFeature | denotes | hypertension |
| T9 | 451-457 | GeneOrGeneProduct | denotes | CYP2C8 |
| T10 | 563-575 | DiseaseOrPhenotypicFeature | denotes | hypertensive |
| T11 | 625-629 | SequenceVariant | denotes | SNPs |
| T12 | 633-639 | GeneOrGeneProduct | denotes | CYP2C8 |
| T13 | 744-756 | DiseaseOrPhenotypicFeature | denotes | hypertension |
| T14 | 842-860 | SequenceVariant | denotes | T deletion at 5063 |
| T15 | 865-906 | SequenceVariant | denotes | substitution of C to T at 33468 in exon 8 |
| T16 | 982-994 | DiseaseOrPhenotypicFeature | denotes | hypertensive |
| T17 | 1058-1065 | SequenceVariant | denotes | C35322C |
| T18 | 1127-1139 | SequenceVariant | denotes | SNP at 35322 |
| T19 | 1223-1235 | DiseaseOrPhenotypicFeature | denotes | hypertension |
| T20 | 1379-1383 | SequenceVariant | denotes | SNPs |
| T21 | 1411-1422 | SequenceVariant | denotes | C35322T SNP |
| T22 | 1442-1454 | DiseaseOrPhenotypicFeature | denotes | hypertensive |
biored-valid-gpt-nr-ng
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 23-29 | GeneOrGeneProduct | denotes | CYP2C8 |
| T2 | 33-54 | DiseaseOrPhenotypicFeature | denotes | hypertensive patients |
| T3 | 141-147 | GeneOrGeneProduct | denotes | CYP2C8 |
| T4 | 167-188 | GeneOrGeneProduct | denotes | cytochrome P450 (CYP) |
| T5 | 210-226 | ChemicalEntity | denotes | Arachidonic acid |
| T6 | 247-274 | ChemicalEntity | denotes | epoxyeicosatrienenoic acids |
| T7 | 279-308 | ChemicalEntity | denotes | hydroxyeicosatetrenoic acids, |
| T8 | 337-350 | DiseaseOrPhenotypicFeature | denotes | hypertension. |
| T9 | 451-457 | GeneOrGeneProduct | denotes | CYP2C8 |
| T10 | 532-535 | ChemicalEntity | denotes | DNA |
| T11 | 625-629 | SequenceVariant | denotes | SNPs |
| T12 | 633-639 | GeneOrGeneProduct | denotes | CYP2C8 |
| T13 | 690-696 | GeneOrGeneProduct | denotes | CYP2C8 |
| T14 | 744-756 | DiseaseOrPhenotypicFeature | denotes | hypertension |
| T15 | 842-852 | SequenceVariant | denotes | T deletion |
| T16 | 881-887 | SequenceVariant | denotes | C to T |
| T17 | 1058-1065 | SequenceVariant | denotes | C35322C |
| T18 | 1127-1130 | SequenceVariant | denotes | SNP |
| T19 | 1182-1189 | SequenceVariant | denotes | C35322C |
| T20 | 1223-1236 | DiseaseOrPhenotypicFeature | denotes | hypertension. |
| T21 | 1379-1384 | SequenceVariant | denotes | SNPs. |
| T22 | 1411-1418 | SequenceVariant | denotes | C35322T |
| T23 | 1442-1463 | DiseaseOrPhenotypicFeature | denotes | hypertensive patients |
biored-valid-gpt-nr-g
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 23-29 | GeneOrGeneProduct | denotes | CYP2C8 |
| T2 | 33-45 | DiseaseOrPhenotypicFeature | denotes | hypertensive |
| T3 | 141-147 | GeneOrGeneProduct | denotes | CYP2C8 |
| T4 | 167-182 | GeneOrGeneProduct | denotes | cytochrome P450 |
| T5 | 183-188 | GeneOrGeneProduct | denotes | (CYP) |
| T6 | 210-226 | ChemicalEntity | denotes | Arachidonic acid |
| T7 | 247-274 | ChemicalEntity | denotes | epoxyeicosatrienenoic acids |
| T8 | 279-307 | ChemicalEntity | denotes | hydroxyeicosatetrenoic acids |
| T9 | 337-349 | DiseaseOrPhenotypicFeature | denotes | hypertension |
| T10 | 451-457 | GeneOrGeneProduct | denotes | CYP2C8 |
| T11 | 563-575 | DiseaseOrPhenotypicFeature | denotes | hypertensive |
| T12 | 633-639 | GeneOrGeneProduct | denotes | CYP2C8 |
| T13 | 690-696 | GeneOrGeneProduct | denotes | CYP2C8 |
| T14 | 744-756 | DiseaseOrPhenotypicFeature | denotes | hypertension |
| T15 | 842-860 | SequenceVariant | denotes | T deletion at 5063 |
| T16 | 865-896 | SequenceVariant | denotes | substitution of C to T at 33468 |
| T17 | 982-994 | DiseaseOrPhenotypicFeature | denotes | hypertensive |
| T18 | 1058-1065 | SequenceVariant | denotes | C35322C |
| T19 | 1182-1189 | SequenceVariant | denotes | C35322C |
| T20 | 1223-1235 | DiseaseOrPhenotypicFeature | denotes | hypertension |
| T21 | 1411-1418 | SequenceVariant | denotes | C35322T |
| T22 | 1442-1454 | DiseaseOrPhenotypicFeature | denotes | hypertensive |
biored-valid-gpt-r-ng
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 23-29 | GeneOrGeneProduct | denotes | CYP2C8 |
| T2 | 33-54 | DiseaseOrPhenotypicFeature | denotes | hypertensive patients |
| T3 | 141-147 | GeneOrGeneProduct | denotes | CYP2C8 |
| T4 | 167-188 | GeneOrGeneProduct | denotes | cytochrome P450 (CYP) |
| T5 | 210-226 | ChemicalEntity | denotes | Arachidonic acid |
| T6 | 247-274 | ChemicalEntity | denotes | epoxyeicosatrienenoic acids |
| T7 | 279-307 | ChemicalEntity | denotes | hydroxyeicosatetrenoic acids |
| T8 | 337-349 | DiseaseOrPhenotypicFeature | denotes | hypertension |
| T9 | 451-457 | GeneOrGeneProduct | denotes | CYP2C8 |
| T10 | 532-535 | ChemicalEntity | denotes | DNA |
| T11 | 563-584 | DiseaseOrPhenotypicFeature | denotes | hypertensive patients |
| T12 | 625-629 | SequenceVariant | denotes | SNPs |
| T13 | 633-639 | GeneOrGeneProduct | denotes | CYP2C8 |
| T14 | 690-696 | GeneOrGeneProduct | denotes | CYP2C8 |
| T15 | 744-756 | DiseaseOrPhenotypicFeature | denotes | hypertension |
| T16 | 842-860 | SequenceVariant | denotes | T deletion at 5063 |
| T17 | 865-896 | SequenceVariant | denotes | substitution of C to T at 33468 |
| T18 | 982-1003 | DiseaseOrPhenotypicFeature | denotes | hypertensive patients |
| T19 | 1058-1065 | SequenceVariant | denotes | C35322C |
| T20 | 1127-1130 | SequenceVariant | denotes | SNP |
| T21 | 1182-1189 | SequenceVariant | denotes | C35322C |
| T22 | 1223-1235 | DiseaseOrPhenotypicFeature | denotes | hypertension |
| T23 | 1379-1383 | SequenceVariant | denotes | SNPs |
| T24 | 1411-1418 | SequenceVariant | denotes | C35322T |
| T25 | 1442-1463 | DiseaseOrPhenotypicFeature | denotes | hypertensive patients |
biored-valid-gpt-r-g
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 23-29 | GeneOrGeneProduct | denotes | CYP2C8 |
| T2 | 33-45 | DiseaseOrPhenotypicFeature | denotes | hypertensive |
| T3 | 141-147 | GeneOrGeneProduct | denotes | CYP2C8 |
| T4 | 167-182 | GeneOrGeneProduct | denotes | cytochrome P450 |
| T5 | 210-226 | ChemicalEntity | denotes | Arachidonic acid |
| T6 | 247-274 | ChemicalEntity | denotes | epoxyeicosatrienenoic acids |
| T7 | 279-307 | ChemicalEntity | denotes | hydroxyeicosatetrenoic acids |
| T8 | 337-349 | DiseaseOrPhenotypicFeature | denotes | hypertension |
| T9 | 451-457 | GeneOrGeneProduct | denotes | CYP2C8 |
| T10 | 563-575 | DiseaseOrPhenotypicFeature | denotes | hypertensive |
| T11 | 633-639 | GeneOrGeneProduct | denotes | CYP2C8 |
| T12 | 690-696 | GeneOrGeneProduct | denotes | CYP2C8 |
| T13 | 744-756 | DiseaseOrPhenotypicFeature | denotes | hypertension |
| T14 | 842-860 | SequenceVariant | denotes | T deletion at 5063 |
| T15 | 865-896 | SequenceVariant | denotes | substitution of C to T at 33468 |
| T16 | 982-994 | DiseaseOrPhenotypicFeature | denotes | hypertensive |
| T17 | 1058-1065 | SequenceVariant | denotes | C35322C |
| T18 | 1127-1139 | SequenceVariant | denotes | SNP at 35322 |
| T19 | 1182-1189 | SequenceVariant | denotes | C35322C |
| T20 | 1223-1235 | DiseaseOrPhenotypicFeature | denotes | hypertension |
| T21 | 1411-1418 | SequenceVariant | denotes | C35322T |
| T22 | 1442-1454 | DiseaseOrPhenotypicFeature | denotes | hypertensive |
biored-valid-gemini-nr-g
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 23-29 | GeneOrGeneProduct | denotes | CYP2C8 |
| T2 | 33-45 | DiseaseOrPhenotypicFeature | denotes | hypertensive |
| T3 | 141-147 | GeneOrGeneProduct | denotes | CYP2C8 |
| T4 | 167-182 | GeneOrGeneProduct | denotes | cytochrome P450 |
| T5 | 210-226 | ChemicalEntity | denotes | Arachidonic acid |
| T6 | 247-274 | ChemicalEntity | denotes | epoxyeicosatrienenoic acids |
| T7 | 279-307 | ChemicalEntity | denotes | hydroxyeicosatetrenoic acids |
| T8 | 337-349 | DiseaseOrPhenotypicFeature | denotes | hypertension |
| T9 | 451-457 | GeneOrGeneProduct | denotes | CYP2C8 |
| T10 | 563-575 | DiseaseOrPhenotypicFeature | denotes | hypertensive |
| T11 | 633-639 | GeneOrGeneProduct | denotes | CYP2C8 |
| T12 | 744-756 | DiseaseOrPhenotypicFeature | denotes | hypertension |
| T13 | 842-896 | SequenceVariant | denotes | T deletion at 5063 and substitution of C to T at 33468 |
| T14 | 982-994 | DiseaseOrPhenotypicFeature | denotes | hypertensive |
| T15 | 1058-1065 | SequenceVariant | denotes | C35322C |
| T16 | 1127-1130 | SequenceVariant | denotes | SNP |
| T17 | 1411-1418 | SequenceVariant | denotes | C35322T |
biored-valid-gpt-r-m
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 23-29 | GeneOrGeneProduct | denotes | CYP2C8 |
| T2 | 33-45 | DiseaseOrPhenotypicFeature | denotes | hypertensive |
| T3 | 46-54 | OrganismTaxon | denotes | patients |
| T4 | 141-147 | GeneOrGeneProduct | denotes | CYP2C8 |
| T5 | 210-226 | ChemicalEntity | denotes | Arachidonic acid |
| T6 | 247-274 | ChemicalEntity | denotes | epoxyeicosatrienenoic acids |
| T7 | 279-307 | ChemicalEntity | denotes | hydroxyeicosatetrenoic acids |
| T8 | 337-349 | DiseaseOrPhenotypicFeature | denotes | hypertension |
| T9 | 451-457 | GeneOrGeneProduct | denotes | CYP2C8 |
| T10 | 553-561 | OrganismTaxon | denotes | subjects |
| T11 | 563-575 | DiseaseOrPhenotypicFeature | denotes | hypertensive |
| T12 | 576-584 | OrganismTaxon | denotes | patients |
| T13 | 597-605 | OrganismTaxon | denotes | controls |
| T14 | 625-629 | SequenceVariant | denotes | SNPs |
| T15 | 633-639 | GeneOrGeneProduct | denotes | CYP2C8 |
| T16 | 690-696 | GeneOrGeneProduct | denotes | CYP2C8 |
| T17 | 717-725 | OrganismTaxon | denotes | controls |
| T18 | 730-738 | OrganismTaxon | denotes | patients |
| T19 | 744-756 | DiseaseOrPhenotypicFeature | denotes | hypertension |
| T20 | 842-860 | SequenceVariant | denotes | T deletion at 5063 |
| T21 | 865-896 | SequenceVariant | denotes | substitution of C to T at 33468 |
| T22 | 969-977 | OrganismTaxon | denotes | controls |
| T23 | 982-994 | DiseaseOrPhenotypicFeature | denotes | hypertensive |
| T24 | 995-1003 | OrganismTaxon | denotes | patients |
| T25 | 1058-1065 | SequenceVariant | denotes | C35322C |
| T26 | 1082-1090 | OrganismTaxon | denotes | patients |
| T27 | 1127-1139 | SequenceVariant | denotes | SNP at 35322 |
| T28 | 1182-1189 | SequenceVariant | denotes | C35322C |
| T29 | 1223-1235 | DiseaseOrPhenotypicFeature | denotes | hypertension |
| T30 | 1379-1383 | SequenceVariant | denotes | SNPs |
| T31 | 1411-1418 | SequenceVariant | denotes | C35322T |
| T32 | 1442-1454 | DiseaseOrPhenotypicFeature | denotes | hypertensive |
| T33 | 1455-1463 | OrganismTaxon | denotes | patients |
| T34 | 1477-1485 | OrganismTaxon | denotes | subjects |
biored-valid-gemini-r-m
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 23-29 | GeneOrGeneProduct | denotes | CYP2C8 |
| T2 | 33-45 | DiseaseOrPhenotypicFeature | denotes | hypertensive |
| T3 | 46-54 | OrganismTaxon | denotes | patients |
| T4 | 141-147 | GeneOrGeneProduct | denotes | CYP2C8 |
| T5 | 167-182 | GeneOrGeneProduct | denotes | cytochrome P450 |
| T6 | 210-226 | ChemicalEntity | denotes | Arachidonic acid |
| T7 | 247-274 | ChemicalEntity | denotes | epoxyeicosatrienenoic acids |
| T8 | 279-307 | ChemicalEntity | denotes | hydroxyeicosatetrenoic acids |
| T9 | 337-349 | DiseaseOrPhenotypicFeature | denotes | hypertension |
| T10 | 451-457 | GeneOrGeneProduct | denotes | CYP2C8 |
| T11 | 553-561 | OrganismTaxon | denotes | subjects |
| T12 | 563-575 | DiseaseOrPhenotypicFeature | denotes | hypertensive |
| T13 | 576-584 | OrganismTaxon | denotes | patients |
| T14 | 597-605 | OrganismTaxon | denotes | controls |
| T15 | 625-629 | SequenceVariant | denotes | SNPs |
| T16 | 633-639 | GeneOrGeneProduct | denotes | CYP2C8 |
| T17 | 717-725 | OrganismTaxon | denotes | controls |
| T18 | 730-738 | OrganismTaxon | denotes | patients |
| T19 | 744-756 | DiseaseOrPhenotypicFeature | denotes | hypertension |
| T20 | 842-860 | SequenceVariant | denotes | T deletion at 5063 |
| T21 | 865-896 | SequenceVariant | denotes | substitution of C to T at 33468 |
| T22 | 969-977 | OrganismTaxon | denotes | controls |
| T23 | 982-994 | DiseaseOrPhenotypicFeature | denotes | hypertensive |
| T24 | 995-1003 | OrganismTaxon | denotes | patients |
| T25 | 1058-1065 | SequenceVariant | denotes | C35322C |
| T26 | 1127-1139 | SequenceVariant | denotes | SNP at 35322 |
| T27 | 1182-1189 | SequenceVariant | denotes | C35322C |
| T28 | 1223-1235 | DiseaseOrPhenotypicFeature | denotes | hypertension |
| T29 | 1379-1383 | SequenceVariant | denotes | SNPs |
| T30 | 1411-1422 | SequenceVariant | denotes | C35322T SNP |
| T31 | 1442-1454 | DiseaseOrPhenotypicFeature | denotes | hypertensive |
| T32 | 1455-1463 | OrganismTaxon | denotes | patients |
| T33 | 1469-1476 | OrganismTaxon | denotes | control |
| T34 | 1477-1485 | OrganismTaxon | denotes | subjects |
biored-valid-deepseek-r-m
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 23-29 | GeneOrGeneProduct | denotes | CYP2C8 |
| T2 | 33-45 | DiseaseOrPhenotypicFeature | denotes | hypertensive |
| T3 | 141-147 | GeneOrGeneProduct | denotes | CYP2C8 |
| T4 | 167-182 | GeneOrGeneProduct | denotes | cytochrome P450 |
| T5 | 210-226 | ChemicalEntity | denotes | Arachidonic acid |
| T6 | 247-274 | ChemicalEntity | denotes | epoxyeicosatrienenoic acids |
| T7 | 279-307 | ChemicalEntity | denotes | hydroxyeicosatetrenoic acids |
| T8 | 337-349 | DiseaseOrPhenotypicFeature | denotes | hypertension |
| T9 | 451-457 | GeneOrGeneProduct | denotes | CYP2C8 |
| T10 | 563-575 | DiseaseOrPhenotypicFeature | denotes | hypertensive |
| T11 | 625-629 | SequenceVariant | denotes | SNPs |
| T12 | 744-756 | DiseaseOrPhenotypicFeature | denotes | hypertension |
| T13 | 801-809 | SequenceVariant | denotes | variants |
| T14 | 842-860 | SequenceVariant | denotes | T deletion at 5063 |
| T15 | 865-906 | SequenceVariant | denotes | substitution of C to T at 33468 in exon 8 |
| T16 | 982-994 | DiseaseOrPhenotypicFeature | denotes | hypertensive |
| T17 | 1058-1065 | SequenceVariant | denotes | C35322C |
| T18 | 1127-1139 | SequenceVariant | denotes | SNP at 35322 |
| T19 | 1411-1418 | SequenceVariant | denotes | C35322T |