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LitCoin-entities

Id Subject Object Predicate Lexical cue db_id
7545 35-55 GeneOrGeneProduct denotes phosphodiesterase 4D NCBIGene:5144
7546 57-62 GeneOrGeneProduct denotes PDE4D NCBIGene:5144
7547 67-90 DiseaseOrPhenotypicFeature denotes carotid atherosclerosis MESH:D002340
7548 108-128 GeneOrGeneProduct denotes phosphodiesterase 4D NCBIGene:5144
7549 130-135 GeneOrGeneProduct denotes PDE4D NCBIGene:5144
7550 183-189 DiseaseOrPhenotypicFeature denotes stroke MESH:D020521
7551 260-271 DiseaseOrPhenotypicFeature denotes atherogenic MESH:D050197
7552 460-475 DiseaseOrPhenotypicFeature denotes atherosclerosis MESH:D050197
7553 532-538 DiseaseOrPhenotypicFeature denotes stroke MESH:D020521
7554 629-632 OrganismTaxon denotes men NCBITaxon:9606
7555 983-986 OrganismTaxon denotes men NCBITaxon:9606
7556 991-996 OrganismTaxon denotes women NCBITaxon:9606
7557 1078-1086 SequenceVariant denotes Rs702553 DBSNP:rs702553
7558 1094-1099 GeneOrGeneProduct denotes PDE4D NCBIGene:5144
7559 1156-1162 DiseaseOrPhenotypicFeature denotes stroke MESH:D020521
7560 1202-1208 DiseaseOrPhenotypicFeature denotes stroke MESH:D020521
7561 1421-1429 SequenceVariant denotes rs702553 DBSNP:rs702553
7562 1568-1571 OrganismTaxon denotes men NCBITaxon:9606
7563 1583-1588 OrganismTaxon denotes women NCBITaxon:9606
7564 1770-1773 OrganismTaxon denotes men NCBITaxon:9606
7565 1909-1914 OrganismTaxon denotes women NCBITaxon:9606
7566 1965-1973 SequenceVariant denotes rs702553 DBSNP:rs702553
7567 1990-1998 SequenceVariant denotes rs702553 DBSNP:rs702553
7568 2029-2035 DiseaseOrPhenotypicFeature denotes stroke MESH:D020521
7569 2036-2039 OrganismTaxon denotes men NCBITaxon:9606
7570 2073-2078 OrganismTaxon denotes women NCBITaxon:9606
7571 2164-2169 GeneOrGeneProduct denotes PDE4D NCBIGene:5144
7572 2195-2201 DiseaseOrPhenotypicFeature denotes stroke MESH:D020521
7573 2256-2269 DiseaseOrPhenotypicFeature denotes atherogenesis MESH:D050197

LitCoin-sentences

Id Subject Object Predicate Lexical cue
T1 0-91 Sentence denotes Sex-differential genetic effect of phosphodiesterase 4D (PDE4D) on carotid atherosclerosis.
T2 92-103 Sentence denotes BACKGROUND:
T3 104-190 Sentence denotes The phosphodiesterase 4D (PDE4D) gene was reported as a susceptibility gene to stroke.
T4 191-304 Sentence denotes The genetic effect might be attributed to its role in modulating the atherogenic process in the carotid arteries.
T5 305-476 Sentence denotes Using carotid intima-media thickness (IMT) and plaque index as phenotypes, the present study sought to determine the influence of this gene on subclinical atherosclerosis.
T6 477-485 Sentence denotes METHODS:
T7 486-634 Sentence denotes Carotid ultrasonography was performed on 1013 stroke-free subjects who participated in the health screening programs (age 52.6 +/- 12.2; 47.6% men).
T8 635-772 Sentence denotes Genotype distribution was compared among the high-risk (plaque index > or = 4), low-risk (index = 1-3), and reference (index = 0) groups.
T9 773-898 Sentence denotes We analyzed continuous IMT data and further dichotomized IMT data using mean plus one standard deviation as the cutoff level.
T10 899-1077 Sentence denotes Because the plaque prevalence and IMT values displayed a notable difference between men and women, we carried out sex-specific analyses in addition to analyzing the overall data.
T11 1078-1186 Sentence denotes Rs702553 at the PDE4D gene was selected because it conferred a risk for young stroke in our previous report.
T12 1187-1363 Sentence denotes Previous young stroke data (190 cases and 211 controls) with an additional 532 control subjects without ultrasonic data were shown as a cross-validation for the genetic effect.
T13 1364-1372 Sentence denotes RESULTS:
T14 1373-1490 Sentence denotes In the overall analyses, the rare homozygote of rs702553 led to an OR of 3.1 (p = 0.034) for a plaque index > or = 4.
T15 1491-1589 Sentence denotes When subjects were stratified by sex, the genetic effect was only evident in men but not in women.
T16 1590-1740 Sentence denotes Comparing male subjects with plaque index > or = 4 and those with plaque index = 0, the TT genotype was over-represented (27.6% vs. 13.4%, p = 0.008).
T17 1741-1905 Sentence denotes For dichotomized IMT data in men, the TT genotype had an OR of 2.1 (p = 0.032) for a thicker IMT at the common carotid artery compared with the (AA + AT) genotypes.
T18 1906-1974 Sentence denotes In women, neither IMT nor plaque index was associated with rs702553.
T19 1975-2090 Sentence denotes Similarly, SNP rs702553 was only significant in young stroke men (OR = 1.8, p = 0.025) but not in women (p = 0.27).
T20 2091-2103 Sentence denotes CONCLUSIONS:
T21 2104-2270 Sentence denotes The present study demonstrates a sex-differential effect of PDE4D on IMT, plaque index and stroke, which highlights its influence on various aspects of atherogenesis.

LitCoin_Mondo

Id Subject Object Predicate Lexical cue mondo_id
T1 75-90 DiseaseOrPhenotypicFeature denotes atherosclerosis 0005311
T2 460-475 DiseaseOrPhenotypicFeature denotes atherosclerosis 0005311
T3 1402-1406 DiseaseOrPhenotypicFeature denotes rare 0021136

LitCoin-SeqVar

Id Subject Object Predicate Lexical cue
T1 1421-1429 SequenceVariant denotes rs702553
T2 1965-1973 SequenceVariant denotes rs702553
T3 1990-1998 SequenceVariant denotes rs702553

LitCoin-GeneOrGeneProduct-v0

Id Subject Object Predicate Lexical cue
T1 35-55 GeneOrGeneProduct denotes phosphodiesterase 4D
T2 57-62 GeneOrGeneProduct denotes PDE4D
T3 108-128 GeneOrGeneProduct denotes phosphodiesterase 4D
T4 130-135 GeneOrGeneProduct denotes PDE4D
T5 272-282 GeneOrGeneProduct denotes process in
T6 326-331 GeneOrGeneProduct denotes media
T7 332-341 GeneOrGeneProduct denotes thickness
T8 408-417 GeneOrGeneProduct denotes determine
T9 477-484 GeneOrGeneProduct denotes METHODS
T10 680-684 GeneOrGeneProduct denotes high
T11 706-712 GeneOrGeneProduct denotes or = 4
T12 885-891 GeneOrGeneProduct denotes cutoff
T13 937-943 GeneOrGeneProduct denotes values
T14 1009-1012 GeneOrGeneProduct denotes out
T15 1094-1099 GeneOrGeneProduct denotes PDE4D
T16 1150-1155 GeneOrGeneProduct denotes young
T17 1196-1201 GeneOrGeneProduct denotes young
T18 1219-1224 GeneOrGeneProduct denotes cases
T19 1402-1406 GeneOrGeneProduct denotes rare
T20 1483-1489 GeneOrGeneProduct denotes or = 4
T21 1600-1604 GeneOrGeneProduct denotes male
T22 1634-1640 GeneOrGeneProduct denotes or = 4
T23 1798-1807 GeneOrGeneProduct denotes OR of 2.1
T24 1975-1984 GeneOrGeneProduct denotes Similarly
T25 2023-2028 GeneOrGeneProduct denotes young
T26 2164-2169 GeneOrGeneProduct denotes PDE4D

LitCoin-GeneOrGeneProduct-v2

Id Subject Object Predicate Lexical cue
T1 35-55 GeneOrGeneProduct denotes phosphodiesterase 4D
T2 57-62 GeneOrGeneProduct denotes PDE4D
T3 108-128 GeneOrGeneProduct denotes phosphodiesterase 4D
T4 130-135 GeneOrGeneProduct denotes PDE4D
T5 326-331 GeneOrGeneProduct denotes media
T6 680-684 GeneOrGeneProduct denotes high
T7 885-891 GeneOrGeneProduct denotes cutoff
T8 1094-1099 GeneOrGeneProduct denotes PDE4D
T9 1150-1155 GeneOrGeneProduct denotes young
T10 1196-1201 GeneOrGeneProduct denotes young
T11 1402-1406 GeneOrGeneProduct denotes rare
T12 2023-2028 GeneOrGeneProduct denotes young
T13 2164-2169 GeneOrGeneProduct denotes PDE4D

LitCoin-Disease-MeSH

Id Subject Object Predicate Lexical cue originalLabel
T1 67-90 DiseaseOrPhenotypicFeature denotes carotid atherosclerosis D002340
T2 183-189 DiseaseOrPhenotypicFeature denotes stroke D020521
T3 260-271 DiseaseOrPhenotypicFeature denotes atherogenic DISEASE
T4 460-475 DiseaseOrPhenotypicFeature denotes atherosclerosis D050197
T5 532-538 DiseaseOrPhenotypicFeature denotes stroke D020521
T6 1156-1162 DiseaseOrPhenotypicFeature denotes stroke D020521
T7 1202-1208 DiseaseOrPhenotypicFeature denotes stroke D020521
T8 2029-2035 DiseaseOrPhenotypicFeature denotes stroke D020521
T9 2195-2201 DiseaseOrPhenotypicFeature denotes stroke D020521
T10 2256-2269 DiseaseOrPhenotypicFeature denotes atherogenesis D050197

LitCoin-GeneOrGeneProduct-v3

Id Subject Object Predicate Lexical cue
T1 35-55 GeneOrGeneProduct denotes phosphodiesterase 4D
T2 57-62 GeneOrGeneProduct denotes PDE4D
T3 108-128 GeneOrGeneProduct denotes phosphodiesterase 4D
T4 130-135 GeneOrGeneProduct denotes PDE4D
T5 885-891 GeneOrGeneProduct denotes cutoff
T6 1094-1099 GeneOrGeneProduct denotes PDE4D
T7 2164-2169 GeneOrGeneProduct denotes PDE4D

LitCoin_Mondo_095

Id Subject Object Predicate Lexical cue mondo_id
T1 75-90 DiseaseOrPhenotypicFeature denotes atherosclerosis 0005311
T2 183-189 DiseaseOrPhenotypicFeature denotes stroke 0005098
T3 343-346 DiseaseOrPhenotypicFeature denotes IMT 0015798
T4 460-475 DiseaseOrPhenotypicFeature denotes atherosclerosis 0005311
T5 532-538 DiseaseOrPhenotypicFeature denotes stroke 0005098
T6 629-632 DiseaseOrPhenotypicFeature denotes men 0017169
T7 796-799 DiseaseOrPhenotypicFeature denotes IMT 0015798
T8 830-833 DiseaseOrPhenotypicFeature denotes IMT 0015798
T9 933-936 DiseaseOrPhenotypicFeature denotes IMT 0015798
T10 983-986 DiseaseOrPhenotypicFeature denotes men 0017169
T11 1156-1162 DiseaseOrPhenotypicFeature denotes stroke 0005098
T12 1202-1208 DiseaseOrPhenotypicFeature denotes stroke 0005098
T13 1568-1571 DiseaseOrPhenotypicFeature denotes men 0017169
T14 1758-1761 DiseaseOrPhenotypicFeature denotes IMT 0015798
T15 1770-1773 DiseaseOrPhenotypicFeature denotes men 0017169
T16 1834-1837 DiseaseOrPhenotypicFeature denotes IMT 0015798
T17 1924-1927 DiseaseOrPhenotypicFeature denotes IMT 0015798
T18 2029-2035 DiseaseOrPhenotypicFeature denotes stroke 0005098
T19 2036-2039 DiseaseOrPhenotypicFeature denotes men 0017169
T20 2173-2176 DiseaseOrPhenotypicFeature denotes IMT 0015798
T21 2195-2201 DiseaseOrPhenotypicFeature denotes stroke 0005098

LitCoin-MeSH-Disease-2

Id Subject Object Predicate Lexical cue ID:
T1 67-90 DiseaseOrPhenotypicFeature denotes carotid atherosclerosis D002340
T2 183-189 DiseaseOrPhenotypicFeature denotes stroke DISEASE|D020521
T4 260-271 DiseaseOrPhenotypicFeature denotes atherogenic DISEASE
T5 460-475 DiseaseOrPhenotypicFeature denotes atherosclerosis D050197
T6 532-538 DiseaseOrPhenotypicFeature denotes stroke DISEASE|D020521
T8 1156-1162 DiseaseOrPhenotypicFeature denotes stroke DISEASE|D020521
T10 1202-1208 DiseaseOrPhenotypicFeature denotes stroke DISEASE|D020521
T12 2029-2035 DiseaseOrPhenotypicFeature denotes stroke DISEASE|D020521
T14 2195-2201 DiseaseOrPhenotypicFeature denotes stroke DISEASE|D020521
T16 2256-2269 DiseaseOrPhenotypicFeature denotes atherogenesis D050197

LitCoin-NCBITaxon-2

Id Subject Object Predicate Lexical cue
T1 629-632 OrganismTaxon denotes men
T2 983-986 OrganismTaxon denotes men
T3 991-996 OrganismTaxon denotes women
T4 1568-1571 OrganismTaxon denotes men
T5 1583-1588 OrganismTaxon denotes women
T6 1770-1773 OrganismTaxon denotes men
T7 1909-1914 OrganismTaxon denotes women
T8 2036-2039 OrganismTaxon denotes men
T9 2073-2078 OrganismTaxon denotes women

LitCoin-MONDO_bioort2019

Id Subject Object Predicate Lexical cue #label
T1 67-90 DiseaseOrPhenotypicFeature denotes carotid atherosclerosis D002340
T2 183-189 DiseaseOrPhenotypicFeature denotes stroke D020521
T3 260-271 DiseaseOrPhenotypicFeature denotes atherogenic DISEASE
T4 460-475 DiseaseOrPhenotypicFeature denotes atherosclerosis D050197
T5 532-538 DiseaseOrPhenotypicFeature denotes stroke D020521
T6 1156-1162 DiseaseOrPhenotypicFeature denotes stroke D020521
T7 1202-1208 DiseaseOrPhenotypicFeature denotes stroke D020521
T8 2029-2035 DiseaseOrPhenotypicFeature denotes stroke D020521
T9 2195-2201 DiseaseOrPhenotypicFeature denotes stroke D020521
T10 2256-2269 DiseaseOrPhenotypicFeature denotes atherogenesis D050197

LitCoin-Chemical-MeSH-CHEBI

Id Subject Object Predicate Lexical cue ID:
T1 35-52 ChemicalEntity denotes phosphodiesterase D010727
T2 108-125 ChemicalEntity denotes phosphodiesterase D010727

LitCoin-training-merged

Id Subject Object Predicate Lexical cue #label ID:
T2 108-125 ChemicalEntity denotes phosphodiesterase D010727
T1 35-52 ChemicalEntity denotes phosphodiesterase D010727
T7 2164-2169 GeneOrGeneProduct denotes PDE4D
T6 1094-1099 GeneOrGeneProduct denotes PDE4D
T5 885-891 GeneOrGeneProduct denotes cutoff
T4 130-135 GeneOrGeneProduct denotes PDE4D
T3 108-128 GeneOrGeneProduct denotes phosphodiesterase 4D
T20700 57-62 GeneOrGeneProduct denotes PDE4D
T17844 35-55 GeneOrGeneProduct denotes phosphodiesterase 4D
T10 2256-2269 DiseaseOrPhenotypicFeature denotes atherogenesis D050197
T9 2195-2201 DiseaseOrPhenotypicFeature denotes stroke D020521
T8 2029-2035 DiseaseOrPhenotypicFeature denotes stroke D020521
T95667 1202-1208 DiseaseOrPhenotypicFeature denotes stroke D020521
T65416 1156-1162 DiseaseOrPhenotypicFeature denotes stroke D020521
T86255 532-538 DiseaseOrPhenotypicFeature denotes stroke D020521
T85028 460-475 DiseaseOrPhenotypicFeature denotes atherosclerosis D050197
T89601 260-271 DiseaseOrPhenotypicFeature denotes atherogenic DISEASE
T20574 183-189 DiseaseOrPhenotypicFeature denotes stroke D020521
T50333 67-90 DiseaseOrPhenotypicFeature denotes carotid atherosclerosis D002340
T71394 2073-2078 OrganismTaxon denotes women
T50813 2036-2039 OrganismTaxon denotes men
T57784 1909-1914 OrganismTaxon denotes women
T38231 1770-1773 OrganismTaxon denotes men
T67414 1583-1588 OrganismTaxon denotes women
T81591 1568-1571 OrganismTaxon denotes men
T14055 991-996 OrganismTaxon denotes women
T42261 983-986 OrganismTaxon denotes men
T17795 629-632 OrganismTaxon denotes men
T84871 1990-1998 SequenceVariant denotes rs702553
T69829 1965-1973 SequenceVariant denotes rs702553
T70878 1421-1429 SequenceVariant denotes rs702553

PubmedHPO

Id Subject Object Predicate Lexical cue
T1 183-189 HP_0001297 denotes stroke
T2 460-475 HP_0002621 denotes atherosclerosis

Allie

Id Subject Object Predicate Lexical cue
SS1_20540798_0_0 35-55 expanded denotes phosphodiesterase 4D
SS2_20540798_0_0 57-62 abbr denotes PDE4D
SS1_20540798_2_0 108-128 expanded denotes phosphodiesterase 4D
SS2_20540798_2_0 130-135 abbr denotes PDE4D
SS1_20540798_4_0 319-341 expanded denotes intima-media thickness
SS2_20540798_4_0 343-346 abbr denotes IMT
AE1_20540798_0_0 SS1_20540798_0_0 SS2_20540798_0_0 abbreviatedTo phosphodiesterase 4D,PDE4D
AE1_20540798_2_0 SS1_20540798_2_0 SS2_20540798_2_0 abbreviatedTo phosphodiesterase 4D,PDE4D
AE1_20540798_4_0 SS1_20540798_4_0 SS2_20540798_4_0 abbreviatedTo intima-media thickness,IMT

biored-valid

Id Subject Object Predicate Lexical cue
T1 35-55 GeneOrGeneProduct denotes phosphodiesterase 4D
T2 57-62 GeneOrGeneProduct denotes PDE4D
T3 67-90 DiseaseOrPhenotypicFeature denotes carotid atherosclerosis
T4 108-128 GeneOrGeneProduct denotes phosphodiesterase 4D
T5 130-135 GeneOrGeneProduct denotes PDE4D
T6 183-189 DiseaseOrPhenotypicFeature denotes stroke
T7 260-271 DiseaseOrPhenotypicFeature denotes atherogenic
T8 460-475 DiseaseOrPhenotypicFeature denotes atherosclerosis
T9 532-538 DiseaseOrPhenotypicFeature denotes stroke
T10 629-632 OrganismTaxon denotes men
T11 983-986 OrganismTaxon denotes men
T12 991-996 OrganismTaxon denotes women
T13 1078-1086 SequenceVariant denotes Rs702553
T14 1094-1099 GeneOrGeneProduct denotes PDE4D
T15 1156-1162 DiseaseOrPhenotypicFeature denotes stroke
T16 1202-1208 DiseaseOrPhenotypicFeature denotes stroke
T17 1421-1429 SequenceVariant denotes rs702553
T18 1568-1571 OrganismTaxon denotes men
T19 1583-1588 OrganismTaxon denotes women
T20 1770-1773 OrganismTaxon denotes men
T21 1909-1914 OrganismTaxon denotes women
T22 1965-1973 SequenceVariant denotes rs702553
T23 1990-1998 SequenceVariant denotes rs702553
T24 2029-2035 DiseaseOrPhenotypicFeature denotes stroke
T25 2036-2039 OrganismTaxon denotes men
T26 2073-2078 OrganismTaxon denotes women
T27 2164-2169 GeneOrGeneProduct denotes PDE4D
T28 2195-2201 DiseaseOrPhenotypicFeature denotes stroke
T29 2256-2269 DiseaseOrPhenotypicFeature denotes atherogenesis

biored-valid-deepseek-nr-ng

Id Subject Object Predicate Lexical cue
T1 57-62 GeneOrGeneProduct denotes PDE4D
T2 67-90 DiseaseOrPhenotypicFeature denotes carotid atherosclerosis
T3 183-189 DiseaseOrPhenotypicFeature denotes stroke
T4 311-341 DiseaseOrPhenotypicFeature denotes carotid intima-media thickness
T5 352-358 DiseaseOrPhenotypicFeature denotes plaque
T6 448-475 DiseaseOrPhenotypicFeature denotes subclinical atherosclerosis
T7 486-509 DiseaseOrPhenotypicFeature denotes Carotid ultrasonography
T8 532-538 DiseaseOrPhenotypicFeature denotes stroke
T9 691-697 DiseaseOrPhenotypicFeature denotes plaque
T10 796-799 DiseaseOrPhenotypicFeature denotes IMT
T11 911-917 DiseaseOrPhenotypicFeature denotes plaque
T12 933-936 DiseaseOrPhenotypicFeature denotes IMT
T13 1078-1086 SequenceVariant denotes Rs702553
T14 1094-1099 GeneOrGeneProduct denotes PDE4D
T15 1150-1162 DiseaseOrPhenotypicFeature denotes young stroke
T16 1202-1208 DiseaseOrPhenotypicFeature denotes stroke
T17 1468-1474 DiseaseOrPhenotypicFeature denotes plaque

biored-valid-deepseek-nr-g

Id Subject Object Predicate Lexical cue
T1 17-21 GeneOrGeneProduct denotes gene
T2 57-62 GeneOrGeneProduct denotes PDE4D
T3 67-74 DiseaseOrPhenotypicFeature denotes carotid
T4 75-90 DiseaseOrPhenotypicFeature denotes atherosclerosis
T5 130-135 GeneOrGeneProduct denotes PDE4D
T6 137-141 GeneOrGeneProduct denotes gene
T7 146-152 DiseaseOrPhenotypicFeature denotes report
T8 183-189 DiseaseOrPhenotypicFeature denotes stroke
T9 195-202 DiseaseOrPhenotypicFeature denotes genetic
T10 203-209 DiseaseOrPhenotypicFeature denotes effect
T11 260-271 DiseaseOrPhenotypicFeature denotes atherogenic
T12 295-303 DiseaseOrPhenotypicFeature denotes arteries
T13 311-318 DiseaseOrPhenotypicFeature denotes carotid
T14 319-331 DiseaseOrPhenotypicFeature denotes intima-media
T15 332-341 DiseaseOrPhenotypicFeature denotes thickness
T16 343-346 DiseaseOrPhenotypicFeature denotes IMT
T17 352-358 DiseaseOrPhenotypicFeature denotes plaque
T18 359-364 DiseaseOrPhenotypicFeature denotes index
T19 368-378 DiseaseOrPhenotypicFeature denotes phenotypes
T20 384-391 DiseaseOrPhenotypicFeature denotes present
T21 392-397 DiseaseOrPhenotypicFeature denotes study
T22 398-404 DiseaseOrPhenotypicFeature denotes sought
T23 408-417 DiseaseOrPhenotypicFeature denotes determine
T24 422-431 DiseaseOrPhenotypicFeature denotes influence
T25 440-444 GeneOrGeneProduct denotes gene
T26 448-459 DiseaseOrPhenotypicFeature denotes subclinical
T27 477-484 DiseaseOrPhenotypicFeature denotes METHODS
T28 486-493 DiseaseOrPhenotypicFeature denotes Carotid
T29 494-509 DiseaseOrPhenotypicFeature denotes ultrasonography
T30 514-523 DiseaseOrPhenotypicFeature denotes performed
T31 532-543 DiseaseOrPhenotypicFeature denotes stroke-free
T32 544-552 DiseaseOrPhenotypicFeature denotes subjects
T33 557-569 DiseaseOrPhenotypicFeature denotes participated
T34 577-583 DiseaseOrPhenotypicFeature denotes health
T35 584-593 DiseaseOrPhenotypicFeature denotes screening
T36 594-602 DiseaseOrPhenotypicFeature denotes programs
T37 604-607 DiseaseOrPhenotypicFeature denotes age
T38 629-632 DiseaseOrPhenotypicFeature denotes men
T39 635-643 DiseaseOrPhenotypicFeature denotes Genotype
T40 644-656 DiseaseOrPhenotypicFeature denotes distribution
T41 661-669 DiseaseOrPhenotypicFeature denotes compared
T42 670-675 DiseaseOrPhenotypicFeature denotes among
T43 680-689 DiseaseOrPhenotypicFeature denotes high-risk
T44 691-697 DiseaseOrPhenotypicFeature denotes plaque
T45 698-703 DiseaseOrPhenotypicFeature denotes index
T46 715-723 DiseaseOrPhenotypicFeature denotes low-risk
T47 743-752 DiseaseOrPhenotypicFeature denotes reference
T48 754-759 DiseaseOrPhenotypicFeature denotes index
T49 765-771 DiseaseOrPhenotypicFeature denotes groups
T50 776-784 DiseaseOrPhenotypicFeature denotes analyzed
T51 785-795 DiseaseOrPhenotypicFeature denotes continuous
T52 800-804 DiseaseOrPhenotypicFeature denotes data
T53 809-816 DiseaseOrPhenotypicFeature denotes further
T54 817-829 DiseaseOrPhenotypicFeature denotes dichotomized
T55 830-833 DiseaseOrPhenotypicFeature denotes IMT
T56 834-838 DiseaseOrPhenotypicFeature denotes data
T57 839-844 DiseaseOrPhenotypicFeature denotes using
T58 845-849 DiseaseOrPhenotypicFeature denotes mean
T59 850-854 DiseaseOrPhenotypicFeature denotes plus
T60 855-858 DiseaseOrPhenotypicFeature denotes one
T61 859-867 DiseaseOrPhenotypicFeature denotes standard
T62 868-877 DiseaseOrPhenotypicFeature denotes deviation
T63 885-891 DiseaseOrPhenotypicFeature denotes cutoff
T64 892-897 DiseaseOrPhenotypicFeature denotes level
T65 899-906 DiseaseOrPhenotypicFeature denotes Because
T66 911-917 DiseaseOrPhenotypicFeature denotes plaque
T67 918-928 DiseaseOrPhenotypicFeature denotes prevalence
T68 933-936 DiseaseOrPhenotypicFeature denotes IMT
T69 937-943 DiseaseOrPhenotypicFeature denotes values
T70 944-953 DiseaseOrPhenotypicFeature denotes displayed
T71 956-963 DiseaseOrPhenotypicFeature denotes notable
T72 964-974 DiseaseOrPhenotypicFeature denotes difference
T73 975-982 DiseaseOrPhenotypicFeature denotes between
T74 983-986 DiseaseOrPhenotypicFeature denotes men
T75 991-996 DiseaseOrPhenotypicFeature denotes women
T76 1001-1008 DiseaseOrPhenotypicFeature denotes carried
T77 1013-1025 DiseaseOrPhenotypicFeature denotes sex-specific
T78 1026-1034 DiseaseOrPhenotypicFeature denotes analyses
T79 1038-1046 DiseaseOrPhenotypicFeature denotes addition
T80 1050-1059 DiseaseOrPhenotypicFeature denotes analyzing
T81 1064-1071 DiseaseOrPhenotypicFeature denotes overall
T82 1078-1086 SequenceVariant denotes Rs702553
T83 1094-1099 GeneOrGeneProduct denotes PDE4D
T84 1109-1117 DiseaseOrPhenotypicFeature denotes selected
T85 1118-1125 DiseaseOrPhenotypicFeature denotes because
T86 1129-1138 DiseaseOrPhenotypicFeature denotes conferred
T87 1150-1155 DiseaseOrPhenotypicFeature denotes young
T88 1156-1162 DiseaseOrPhenotypicFeature denotes stroke
T89 1170-1178 DiseaseOrPhenotypicFeature denotes previous
T90 1187-1195 DiseaseOrPhenotypicFeature denotes Previous
T91 1219-1224 DiseaseOrPhenotypicFeature denotes cases
T92 1233-1241 DiseaseOrPhenotypicFeature denotes controls
T93 1251-1261 DiseaseOrPhenotypicFeature denotes additional
T94 1283-1290 DiseaseOrPhenotypicFeature denotes without
T95 1291-1301 DiseaseOrPhenotypicFeature denotes ultrasonic
T96 1312-1317 DiseaseOrPhenotypicFeature denotes shown
T97 1323-1339 DiseaseOrPhenotypicFeature denotes cross-validation
T98 1356-1362 DiseaseOrPhenotypicFeature denotes effect
T99 1364-1371 DiseaseOrPhenotypicFeature denotes RESULTS
T100 1402-1406 DiseaseOrPhenotypicFeature denotes rare
T101 1407-1417 DiseaseOrPhenotypicFeature denotes homozygote
T102 1421-1429 SequenceVariant denotes rs702553
T103 1430-1433 DiseaseOrPhenotypicFeature denotes led
T104 1440-1442 DiseaseOrPhenotypicFeature denotes OR
T105 1510-1520 DiseaseOrPhenotypicFeature denotes stratified
T106 1552-1556 DiseaseOrPhenotypicFeature denotes only
T107 1557-1564 DiseaseOrPhenotypicFeature denotes evident
T108 1590-1599 DiseaseOrPhenotypicFeature denotes Comparing
T109 1600-1604 DiseaseOrPhenotypicFeature denotes male
T110 1645-1650 DiseaseOrPhenotypicFeature denotes those
T111 1678-1680 SequenceVariant denotes TT
T112 1681-1689 SequenceVariant denotes genotype
T113 1694-1710 DiseaseOrPhenotypicFeature denotes over-represented
T114 1826-1833 DiseaseOrPhenotypicFeature denotes thicker
T115 1845-1851 DiseaseOrPhenotypicFeature denotes common
T116 1860-1866 DiseaseOrPhenotypicFeature denotes artery
T117 1886-1888 SequenceVariant denotes AA
T118 1891-1893 SequenceVariant denotes AT
T119 1895-1904 SequenceVariant denotes genotypes
T120 1916-1923 DiseaseOrPhenotypicFeature denotes neither
T121 1949-1959 DiseaseOrPhenotypicFeature denotes associated
T122 1975-1984 DiseaseOrPhenotypicFeature denotes Similarly
T123 1986-1989 SequenceVariant denotes SNP
T124 2008-2019 DiseaseOrPhenotypicFeature denotes significant
T125 2091-2102 DiseaseOrPhenotypicFeature denotes CONCLUSIONS
T126 2122-2134 DiseaseOrPhenotypicFeature denotes demonstrates
T127 2137-2153 DiseaseOrPhenotypicFeature denotes sex-differential
T128 2209-2219 DiseaseOrPhenotypicFeature denotes highlights
T129 2237-2244 DiseaseOrPhenotypicFeature denotes various
T130 2245-2252 DiseaseOrPhenotypicFeature denotes aspects
T131 2256-2269 DiseaseOrPhenotypicFeature denotes atherogenesis

biored-valid-deepseek-r-ng

Id Subject Object Predicate Lexical cue
T1 35-63 GeneOrGeneProduct denotes phosphodiesterase 4D (PDE4D)
T2 67-90 DiseaseOrPhenotypicFeature denotes carotid atherosclerosis
T3 183-189 DiseaseOrPhenotypicFeature denotes stroke
T4 311-341 DiseaseOrPhenotypicFeature denotes carotid intima-media thickness
T5 343-346 DiseaseOrPhenotypicFeature denotes IMT
T6 352-364 DiseaseOrPhenotypicFeature denotes plaque index
T7 448-475 DiseaseOrPhenotypicFeature denotes subclinical atherosclerosis
T8 1094-1099 GeneOrGeneProduct denotes PDE4D
T9 1156-1162 DiseaseOrPhenotypicFeature denotes stroke
T10 1421-1429 SequenceVariant denotes rs702553
T11 1986-1998 SequenceVariant denotes SNP rs702553
T12 2256-2269 DiseaseOrPhenotypicFeature denotes atherogenesis

biored-valid-deepseek-r-g

Id Subject Object Predicate Lexical cue
T1 35-55 GeneOrGeneProduct denotes phosphodiesterase 4D
T2 57-62 GeneOrGeneProduct denotes PDE4D
T3 67-90 DiseaseOrPhenotypicFeature denotes carotid atherosclerosis
T4 108-128 GeneOrGeneProduct denotes phosphodiesterase 4D
T5 130-135 GeneOrGeneProduct denotes PDE4D
T6 183-189 DiseaseOrPhenotypicFeature denotes stroke
T7 311-347 DiseaseOrPhenotypicFeature denotes carotid intima-media thickness (IMT)
T8 448-475 DiseaseOrPhenotypicFeature denotes subclinical atherosclerosis
T9 629-632 OrganismTaxon denotes men
T10 933-936 DiseaseOrPhenotypicFeature denotes IMT
T11 991-996 OrganismTaxon denotes women
T12 1078-1086 SequenceVariant denotes Rs702553
T13 1094-1099 GeneOrGeneProduct denotes PDE4D
T14 1150-1162 DiseaseOrPhenotypicFeature denotes young stroke
T15 1202-1208 DiseaseOrPhenotypicFeature denotes stroke
T16 1421-1429 SequenceVariant denotes rs702553
T17 1678-1689 SequenceVariant denotes TT genotype
T18 1886-1888 SequenceVariant denotes AA
T19 1891-1893 SequenceVariant denotes AT
T20 1986-1998 SequenceVariant denotes SNP rs702553

biored-valid-gemini-nr-ng

Id Subject Object Predicate Lexical cue
T1 35-63 GeneOrGeneProduct denotes phosphodiesterase 4D (PDE4D)
T2 67-90 DiseaseOrPhenotypicFeature denotes carotid atherosclerosis
T3 108-136 GeneOrGeneProduct denotes phosphodiesterase 4D (PDE4D)
T4 183-189 DiseaseOrPhenotypicFeature denotes stroke
T5 260-279 DiseaseOrPhenotypicFeature denotes atherogenic process
T6 311-347 DiseaseOrPhenotypicFeature denotes carotid intima-media thickness (IMT)
T7 352-364 DiseaseOrPhenotypicFeature denotes plaque index
T8 448-475 DiseaseOrPhenotypicFeature denotes subclinical atherosclerosis
T9 532-543 DiseaseOrPhenotypicFeature denotes stroke-free
T10 691-703 DiseaseOrPhenotypicFeature denotes plaque index
T11 796-799 DiseaseOrPhenotypicFeature denotes IMT
T12 830-833 DiseaseOrPhenotypicFeature denotes IMT
T13 911-917 DiseaseOrPhenotypicFeature denotes plaque
T14 1094-1099 GeneOrGeneProduct denotes PDE4D
T15 1150-1162 DiseaseOrPhenotypicFeature denotes young stroke
T16 1421-1429 SequenceVariant denotes rs702553
T17 1468-1480 DiseaseOrPhenotypicFeature denotes plaque index
T18 1619-1631 DiseaseOrPhenotypicFeature denotes plaque index
T19 1758-1761 DiseaseOrPhenotypicFeature denotes IMT
T20 1911-1914 OrganismTaxon denotes men
T21 1924-1927 DiseaseOrPhenotypicFeature denotes IMT
T22 1932-1944 DiseaseOrPhenotypicFeature denotes plaque index
T23 1986-1998 SequenceVariant denotes SNP rs702553
T24 2023-2035 DiseaseOrPhenotypicFeature denotes young stroke
T25 2164-2169 GeneOrGeneProduct denotes PDE4D
T26 2256-2269 DiseaseOrPhenotypicFeature denotes atherogenesis

biored-valid-gemini-r-g

Id Subject Object Predicate Lexical cue
T1 35-55 GeneOrGeneProduct denotes phosphodiesterase 4D
T2 57-62 GeneOrGeneProduct denotes PDE4D
T3 67-90 DiseaseOrPhenotypicFeature denotes carotid atherosclerosis
T4 108-128 GeneOrGeneProduct denotes phosphodiesterase 4D
T5 130-141 GeneOrGeneProduct denotes PDE4D) gene
T6 183-189 DiseaseOrPhenotypicFeature denotes stroke
T7 311-341 DiseaseOrPhenotypicFeature denotes carotid intima-media thickness
T8 343-346 DiseaseOrPhenotypicFeature denotes IMT
T9 352-364 DiseaseOrPhenotypicFeature denotes plaque index
T10 448-475 DiseaseOrPhenotypicFeature denotes subclinical atherosclerosis
T11 532-543 DiseaseOrPhenotypicFeature denotes stroke-free
T12 629-632 OrganismTaxon denotes men
T13 691-703 DiseaseOrPhenotypicFeature denotes plaque index
T14 796-799 DiseaseOrPhenotypicFeature denotes IMT
T15 911-928 DiseaseOrPhenotypicFeature denotes plaque prevalence
T16 983-986 OrganismTaxon denotes men
T17 991-996 OrganismTaxon denotes women
T18 1078-1086 SequenceVariant denotes Rs702553
T19 1094-1104 GeneOrGeneProduct denotes PDE4D gene
T20 1150-1162 DiseaseOrPhenotypicFeature denotes young stroke
T21 1421-1429 SequenceVariant denotes rs702553
T22 1468-1480 DiseaseOrPhenotypicFeature denotes plaque index
T23 1568-1571 OrganismTaxon denotes men
T24 1583-1588 OrganismTaxon denotes women
T25 1600-1604 OrganismTaxon denotes male
T26 1656-1668 DiseaseOrPhenotypicFeature denotes plaque index
T27 1678-1689 SequenceVariant denotes TT genotype
T28 1758-1761 DiseaseOrPhenotypicFeature denotes IMT
T29 1770-1773 OrganismTaxon denotes men
T30 1885-1904 SequenceVariant denotes (AA + AT) genotypes
T31 1909-1914 OrganismTaxon denotes women
T32 1924-1927 DiseaseOrPhenotypicFeature denotes IMT
T33 1932-1944 DiseaseOrPhenotypicFeature denotes plaque index
T34 1965-1973 SequenceVariant denotes rs702553
T35 2023-2035 DiseaseOrPhenotypicFeature denotes young stroke
T36 2164-2169 GeneOrGeneProduct denotes PDE4D

biored-valid-gemini-r-ng

Id Subject Object Predicate Lexical cue
T1 35-63 GeneOrGeneProduct denotes phosphodiesterase 4D (PDE4D)
T2 67-90 DiseaseOrPhenotypicFeature denotes carotid atherosclerosis
T3 108-136 GeneOrGeneProduct denotes phosphodiesterase 4D (PDE4D)
T4 183-189 DiseaseOrPhenotypicFeature denotes stroke
T5 260-279 DiseaseOrPhenotypicFeature denotes atherogenic process
T6 311-347 DiseaseOrPhenotypicFeature denotes carotid intima-media thickness (IMT)
T7 352-364 DiseaseOrPhenotypicFeature denotes plaque index
T8 448-475 DiseaseOrPhenotypicFeature denotes subclinical atherosclerosis
T9 629-632 OrganismTaxon denotes men
T10 691-703 DiseaseOrPhenotypicFeature denotes plaque index
T11 796-799 DiseaseOrPhenotypicFeature denotes IMT
T12 830-833 DiseaseOrPhenotypicFeature denotes IMT
T13 911-928 DiseaseOrPhenotypicFeature denotes plaque prevalence
T14 983-986 OrganismTaxon denotes men
T15 991-996 OrganismTaxon denotes women
T16 1078-1086 SequenceVariant denotes Rs702553
T17 1094-1099 GeneOrGeneProduct denotes PDE4D
T18 1150-1162 DiseaseOrPhenotypicFeature denotes young stroke
T19 1421-1429 SequenceVariant denotes rs702553
T20 1468-1480 DiseaseOrPhenotypicFeature denotes plaque index
T21 1568-1571 OrganismTaxon denotes men
T22 1583-1588 OrganismTaxon denotes women
T23 1600-1604 OrganismTaxon denotes male
T24 1656-1668 DiseaseOrPhenotypicFeature denotes plaque index
T25 1678-1689 SequenceVariant denotes TT genotype
T26 1758-1761 DiseaseOrPhenotypicFeature denotes IMT
T27 1826-1837 DiseaseOrPhenotypicFeature denotes thicker IMT
T28 1885-1904 SequenceVariant denotes (AA + AT) genotypes
T29 1909-1914 OrganismTaxon denotes women
T30 1924-1927 DiseaseOrPhenotypicFeature denotes IMT
T31 1932-1944 DiseaseOrPhenotypicFeature denotes plaque index
T32 1965-1973 SequenceVariant denotes rs702553
T33 2023-2035 DiseaseOrPhenotypicFeature denotes young stroke
T34 2164-2169 GeneOrGeneProduct denotes PDE4D
T35 2256-2269 DiseaseOrPhenotypicFeature denotes atherogenesis

biored-valid-gpt-nr-ng

Id Subject Object Predicate Lexical cue
T1 35-55 GeneOrGeneProduct denotes phosphodiesterase 4D
T2 57-62 GeneOrGeneProduct denotes PDE4D
T3 67-90 DiseaseOrPhenotypicFeature denotes carotid atherosclerosis
T4 108-128 GeneOrGeneProduct denotes phosphodiesterase 4D
T5 130-135 GeneOrGeneProduct denotes PDE4D
T6 183-189 DiseaseOrPhenotypicFeature denotes stroke
T7 319-341 DiseaseOrPhenotypicFeature denotes intima-media thickness
T8 343-346 DiseaseOrPhenotypicFeature denotes IMT
T9 352-364 DiseaseOrPhenotypicFeature denotes plaque index
T10 460-475 DiseaseOrPhenotypicFeature denotes atherosclerosis
T11 796-799 DiseaseOrPhenotypicFeature denotes IMT
T12 1078-1086 SequenceVariant denotes Rs702553
T13 1094-1099 GeneOrGeneProduct denotes PDE4D
T14 1156-1162 DiseaseOrPhenotypicFeature denotes stroke

biored-valid-gpt-nr-g

Id Subject Object Predicate Lexical cue
T1 35-63 GeneOrGeneProduct denotes phosphodiesterase 4D (PDE4D)
T2 67-90 DiseaseOrPhenotypicFeature denotes carotid atherosclerosis
T3 108-136 GeneOrGeneProduct denotes phosphodiesterase 4D (PDE4D)
T4 183-189 DiseaseOrPhenotypicFeature denotes stroke
T5 311-347 DiseaseOrPhenotypicFeature denotes carotid intima-media thickness (IMT)
T6 460-475 DiseaseOrPhenotypicFeature denotes atherosclerosis
T7 1078-1086 SequenceVariant denotes Rs702553
T8 1094-1099 GeneOrGeneProduct denotes PDE4D
T9 1156-1162 DiseaseOrPhenotypicFeature denotes stroke
T10 1421-1429 SequenceVariant denotes rs702553
T11 1678-1689 SequenceVariant denotes TT genotype
T12 1885-1904 SequenceVariant denotes (AA + AT) genotypes
T13 1965-1973 SequenceVariant denotes rs702553
T14 2029-2035 DiseaseOrPhenotypicFeature denotes stroke
T15 2164-2169 GeneOrGeneProduct denotes PDE4D
T16 2195-2201 DiseaseOrPhenotypicFeature denotes stroke

biored-valid-gpt-r-ng

Id Subject Object Predicate Lexical cue
T1 35-63 GeneOrGeneProduct denotes phosphodiesterase 4D (PDE4D)
T2 67-90 DiseaseOrPhenotypicFeature denotes carotid atherosclerosis
T3 108-136 GeneOrGeneProduct denotes phosphodiesterase 4D (PDE4D)
T4 183-189 DiseaseOrPhenotypicFeature denotes stroke
T5 260-279 DiseaseOrPhenotypicFeature denotes atherogenic process
T6 311-347 DiseaseOrPhenotypicFeature denotes carotid intima-media thickness (IMT)
T7 352-364 DiseaseOrPhenotypicFeature denotes plaque index
T8 448-475 DiseaseOrPhenotypicFeature denotes subclinical atherosclerosis
T9 796-799 DiseaseOrPhenotypicFeature denotes IMT
T10 911-928 DiseaseOrPhenotypicFeature denotes plaque prevalence
T11 933-936 DiseaseOrPhenotypicFeature denotes IMT
T12 1078-1086 SequenceVariant denotes Rs702553
T13 1094-1099 GeneOrGeneProduct denotes PDE4D
T14 1150-1162 DiseaseOrPhenotypicFeature denotes young stroke
T15 1421-1429 SequenceVariant denotes rs702553
T16 1468-1480 DiseaseOrPhenotypicFeature denotes plaque index
T17 1619-1631 DiseaseOrPhenotypicFeature denotes plaque index
T18 1678-1689 SequenceVariant denotes TT genotype
T19 1758-1761 DiseaseOrPhenotypicFeature denotes IMT
T20 1779-1790 SequenceVariant denotes TT genotype
T21 1834-1837 DiseaseOrPhenotypicFeature denotes IMT
T22 1885-1904 SequenceVariant denotes (AA + AT) genotypes
T23 1924-1927 DiseaseOrPhenotypicFeature denotes IMT
T24 1932-1944 DiseaseOrPhenotypicFeature denotes plaque index
T25 1965-1973 SequenceVariant denotes rs702553
T26 2023-2035 DiseaseOrPhenotypicFeature denotes young stroke
T27 2164-2169 GeneOrGeneProduct denotes PDE4D
T28 2173-2176 DiseaseOrPhenotypicFeature denotes IMT
T29 2178-2190 DiseaseOrPhenotypicFeature denotes plaque index
T30 2195-2201 DiseaseOrPhenotypicFeature denotes stroke
T31 2256-2269 DiseaseOrPhenotypicFeature denotes atherogenesis

biored-valid-gpt-r-g

Id Subject Object Predicate Lexical cue
T1 35-55 GeneOrGeneProduct denotes phosphodiesterase 4D
T2 57-62 GeneOrGeneProduct denotes PDE4D
T3 75-90 DiseaseOrPhenotypicFeature denotes atherosclerosis
T4 108-128 GeneOrGeneProduct denotes phosphodiesterase 4D
T5 130-135 GeneOrGeneProduct denotes PDE4D
T6 183-189 DiseaseOrPhenotypicFeature denotes stroke
T7 311-341 DiseaseOrPhenotypicFeature denotes carotid intima-media thickness
T8 343-346 DiseaseOrPhenotypicFeature denotes IMT
T9 352-364 DiseaseOrPhenotypicFeature denotes plaque index
T10 460-475 DiseaseOrPhenotypicFeature denotes atherosclerosis
T11 796-799 DiseaseOrPhenotypicFeature denotes IMT
T12 933-936 DiseaseOrPhenotypicFeature denotes IMT
T13 1078-1086 SequenceVariant denotes Rs702553
T14 1094-1099 GeneOrGeneProduct denotes PDE4D
T15 1156-1162 DiseaseOrPhenotypicFeature denotes stroke
T16 1421-1429 SequenceVariant denotes rs702553
T17 1468-1480 DiseaseOrPhenotypicFeature denotes plaque index
T18 1619-1631 DiseaseOrPhenotypicFeature denotes plaque index
T19 1678-1689 SequenceVariant denotes TT genotype
T20 1758-1761 DiseaseOrPhenotypicFeature denotes IMT
T21 1779-1790 SequenceVariant denotes TT genotype
T22 1834-1837 DiseaseOrPhenotypicFeature denotes IMT
T23 1885-1904 SequenceVariant denotes (AA + AT) genotypes
T24 1924-1927 DiseaseOrPhenotypicFeature denotes IMT
T25 1932-1944 DiseaseOrPhenotypicFeature denotes plaque index
T26 1965-1973 SequenceVariant denotes rs702553
T27 2029-2035 DiseaseOrPhenotypicFeature denotes stroke
T28 2164-2169 GeneOrGeneProduct denotes PDE4D
T29 2173-2176 DiseaseOrPhenotypicFeature denotes IMT
T30 2178-2190 DiseaseOrPhenotypicFeature denotes plaque index
T31 2195-2201 DiseaseOrPhenotypicFeature denotes stroke

biored-valid-gemini-nr-g

Id Subject Object Predicate Lexical cue
T1 35-63 GeneOrGeneProduct denotes phosphodiesterase 4D (PDE4D)
T2 67-90 DiseaseOrPhenotypicFeature denotes carotid atherosclerosis
T3 108-136 GeneOrGeneProduct denotes phosphodiesterase 4D (PDE4D)
T4 183-189 DiseaseOrPhenotypicFeature denotes stroke
T5 260-279 DiseaseOrPhenotypicFeature denotes atherogenic process
T6 448-475 DiseaseOrPhenotypicFeature denotes subclinical atherosclerosis
T7 1094-1099 GeneOrGeneProduct denotes PDE4D
T8 1156-1162 DiseaseOrPhenotypicFeature denotes stroke
T9 1421-1429 SequenceVariant denotes rs702553
T10 1965-1973 SequenceVariant denotes rs702553
T11 2029-2035 DiseaseOrPhenotypicFeature denotes stroke
T12 2164-2169 GeneOrGeneProduct denotes PDE4D
T13 2256-2269 DiseaseOrPhenotypicFeature denotes atherogenesis

biored-valid-gpt-r-m

Id Subject Object Predicate Lexical cue
T1 35-55 GeneOrGeneProduct denotes phosphodiesterase 4D
T2 57-62 GeneOrGeneProduct denotes PDE4D
T3 75-90 DiseaseOrPhenotypicFeature denotes atherosclerosis
T4 108-128 GeneOrGeneProduct denotes phosphodiesterase 4D
T5 130-135 GeneOrGeneProduct denotes PDE4D
T6 183-189 DiseaseOrPhenotypicFeature denotes stroke
T7 319-341 DiseaseOrPhenotypicFeature denotes intima-media thickness
T8 343-346 DiseaseOrPhenotypicFeature denotes IMT
T9 352-364 DiseaseOrPhenotypicFeature denotes plaque index
T10 460-475 DiseaseOrPhenotypicFeature denotes atherosclerosis
T11 532-538 DiseaseOrPhenotypicFeature denotes stroke
T12 544-552 OrganismTaxon denotes subjects
T13 691-703 DiseaseOrPhenotypicFeature denotes plaque index
T14 796-799 DiseaseOrPhenotypicFeature denotes IMT
T15 911-928 DiseaseOrPhenotypicFeature denotes plaque prevalence
T16 933-936 DiseaseOrPhenotypicFeature denotes IMT
T17 1078-1086 SequenceVariant denotes Rs702553
T18 1094-1099 GeneOrGeneProduct denotes PDE4D
T19 1156-1162 DiseaseOrPhenotypicFeature denotes stroke
T20 1219-1224 OrganismTaxon denotes cases
T21 1233-1241 OrganismTaxon denotes controls
T22 1274-1282 OrganismTaxon denotes subjects
T23 1421-1429 SequenceVariant denotes rs702553
T24 1468-1480 DiseaseOrPhenotypicFeature denotes plaque index
T25 1496-1504 OrganismTaxon denotes subjects
T26 1605-1613 OrganismTaxon denotes subjects
T27 1619-1631 DiseaseOrPhenotypicFeature denotes plaque index
T28 1678-1680 SequenceVariant denotes TT
T29 1758-1761 DiseaseOrPhenotypicFeature denotes IMT
T30 1779-1781 SequenceVariant denotes TT
T31 1834-1837 DiseaseOrPhenotypicFeature denotes IMT
T32 1886-1888 SequenceVariant denotes AA
T33 1891-1893 SequenceVariant denotes AT
T34 1924-1927 DiseaseOrPhenotypicFeature denotes IMT
T35 1932-1944 DiseaseOrPhenotypicFeature denotes plaque index
T36 1965-1973 SequenceVariant denotes rs702553
T37 2029-2035 DiseaseOrPhenotypicFeature denotes stroke
T38 2164-2169 GeneOrGeneProduct denotes PDE4D
T39 2173-2176 DiseaseOrPhenotypicFeature denotes IMT
T40 2178-2190 DiseaseOrPhenotypicFeature denotes plaque index
T41 2195-2201 DiseaseOrPhenotypicFeature denotes stroke

biored-valid-gemini-r-m

Id Subject Object Predicate Lexical cue
T1 35-55 GeneOrGeneProduct denotes phosphodiesterase 4D
T2 57-62 GeneOrGeneProduct denotes PDE4D
T3 67-90 DiseaseOrPhenotypicFeature denotes carotid atherosclerosis
T4 108-136 GeneOrGeneProduct denotes phosphodiesterase 4D (PDE4D)
T5 183-189 DiseaseOrPhenotypicFeature denotes stroke
T6 319-341 DiseaseOrPhenotypicFeature denotes intima-media thickness
T7 343-346 DiseaseOrPhenotypicFeature denotes IMT
T8 460-475 DiseaseOrPhenotypicFeature denotes atherosclerosis
T9 544-552 OrganismTaxon denotes subjects
T10 629-632 OrganismTaxon denotes men
T11 983-986 OrganismTaxon denotes men
T12 991-996 OrganismTaxon denotes women
T13 1078-1086 SequenceVariant denotes Rs702553
T14 1094-1099 GeneOrGeneProduct denotes PDE4D
T15 1156-1162 DiseaseOrPhenotypicFeature denotes stroke
T16 1219-1224 OrganismTaxon denotes cases
T17 1233-1241 OrganismTaxon denotes controls
T18 1266-1282 OrganismTaxon denotes control subjects
T19 1421-1429 SequenceVariant denotes rs702553
T20 1568-1571 OrganismTaxon denotes men
T21 1583-1588 OrganismTaxon denotes women
T22 1600-1613 OrganismTaxon denotes male subjects
T23 1678-1680 SequenceVariant denotes TT
T24 1758-1761 DiseaseOrPhenotypicFeature denotes IMT
T25 1770-1773 OrganismTaxon denotes men
T26 1826-1837 DiseaseOrPhenotypicFeature denotes thicker IMT
T27 1886-1888 SequenceVariant denotes AA
T28 1891-1893 SequenceVariant denotes AT
T29 1909-1914 OrganismTaxon denotes women
T30 1965-1973 SequenceVariant denotes rs702553
T31 1986-1998 SequenceVariant denotes SNP rs702553
T32 2029-2035 DiseaseOrPhenotypicFeature denotes stroke
T33 2164-2169 GeneOrGeneProduct denotes PDE4D

biored-valid-deepseek-r-m

Id Subject Object Predicate Lexical cue
T1 35-63 GeneOrGeneProduct denotes phosphodiesterase 4D (PDE4D)
T2 67-90 DiseaseOrPhenotypicFeature denotes carotid atherosclerosis
T3 108-141 GeneOrGeneProduct denotes phosphodiesterase 4D (PDE4D) gene
T4 183-189 DiseaseOrPhenotypicFeature denotes stroke
T5 311-347 DiseaseOrPhenotypicFeature denotes carotid intima-media thickness (IMT)
T6 352-364 DiseaseOrPhenotypicFeature denotes plaque index
T7 448-475 DiseaseOrPhenotypicFeature denotes subclinical atherosclerosis
T8 1078-1086 SequenceVariant denotes Rs702553
T9 1094-1099 GeneOrGeneProduct denotes PDE4D
T10 1150-1162 DiseaseOrPhenotypicFeature denotes young stroke
T11 1421-1429 SequenceVariant denotes rs702553
T12 1678-1689 SequenceVariant denotes TT genotype