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LitCoin-sentences

Id Subject Object Predicate Lexical cue
T1 0-112 Sentence denotes Vitamin E reduces cardiovascular disease in individuals with diabetes mellitus and the haptoglobin 2-2 genotype.
T2 113-118 Sentence denotes AIMS:
T3 119-250 Sentence denotes Individuals with both diabetes mellitus (DM) and the Haptoglobin (Hp) 2-2 genotype are at increased risk of cardiovascular disease.
T4 251-471 Sentence denotes As the antioxidant function of the Hp 2-2 protein is impaired, we sought to test the pharmacogenomic hypothesis that antioxidant vitamin E supplementation would provide cardiovascular protection to Hp 2-2 DM individuals.
T5 472-492 Sentence denotes MATERIALS & METHODS:
T6 493-737 Sentence denotes We determined the Hp genotype on DM participants from two trials (HOPE and ICARE) and assessed the effect of vitamin E by Hp genotype on their common prespecified outcome, the composite of stroke, myocardial infarction and cardiovascular death.
T7 738-782 Sentence denotes Data was analyzed with a fixed-effect model.
T8 783-983 Sentence denotes These results were input into a simulation model, the Evidence Based Medicine Integrator, in order to estimate their long-term implications in a real-world population from Kaiser Permanente (CA, USA).
T9 984-992 Sentence denotes RESULTS:
T10 993-1149 Sentence denotes Meta-analysis of the two trials demonstrated a significant overall reduction in the composite end point in Hp 2-2 DM individuals with vitamin E (odds ratio:
T11 1150-1163 Sentence denotes 0.58; 95% CI:
T12 1164-1186 Sentence denotes 0.40-0.86; p = 0.006).
T13 1187-1302 Sentence denotes There was a statistically significant interaction between the Hp genotype and vitamin E on the composite end point.
T14 1303-1466 Sentence denotes In these trials, Hp typing of 69 DM individuals and treating those with the Hp 2-2 with vitamin E prevented one myocardial infarct, stroke or cardiovascular death.
T15 1467-1602 Sentence denotes Lifelong administration of vitamin E to Hp 2-2 DM individuals in the Kaiser population would increase their life expectancy by 3 years.
T16 1603-1614 Sentence denotes CONCLUSION:
T17 1615-1778 Sentence denotes A pharmacogenomic strategy of screening DM individuals for the Hp genotype and treating those with Hp 2-2 with vitamin E appears to be highly clinically effective.

LitCoin-entities

Id Subject Object Predicate Lexical cue db_id
7220 0-9 ChemicalEntity denotes Vitamin E MESH:D014810
7221 18-40 DiseaseOrPhenotypicFeature denotes cardiovascular disease MESH:D002318
7222 61-78 DiseaseOrPhenotypicFeature denotes diabetes mellitus MESH:D003920
7223 87-98 GeneOrGeneProduct denotes haptoglobin NCBIGene:3240
7224 141-158 DiseaseOrPhenotypicFeature denotes diabetes mellitus MESH:D003920
7225 160-162 DiseaseOrPhenotypicFeature denotes DM MESH:D003920
7226 172-183 GeneOrGeneProduct denotes Haptoglobin NCBIGene:3240
7227 185-187 GeneOrGeneProduct denotes Hp NCBIGene:3240
7228 227-249 DiseaseOrPhenotypicFeature denotes cardiovascular disease MESH:D002318
7229 286-288 GeneOrGeneProduct denotes Hp NCBIGene:3240
7230 368-379 ChemicalEntity denotes antioxidant MESH:D000975
7231 380-389 ChemicalEntity denotes vitamin E MESH:D014810
7232 449-451 GeneOrGeneProduct denotes Hp NCBIGene:3240
7233 456-458 DiseaseOrPhenotypicFeature denotes DM MESH:D003920
7234 511-513 GeneOrGeneProduct denotes Hp NCBIGene:3240
7235 526-528 DiseaseOrPhenotypicFeature denotes DM MESH:D003920
7236 602-611 ChemicalEntity denotes vitamin E MESH:D014810
7237 615-617 GeneOrGeneProduct denotes Hp NCBIGene:3240
7238 682-688 DiseaseOrPhenotypicFeature denotes stroke MESH:D020521
7239 690-711 DiseaseOrPhenotypicFeature denotes myocardial infarction MESH:D009203
7240 716-736 DiseaseOrPhenotypicFeature denotes cardiovascular death MESH:D002318
7241 1100-1102 GeneOrGeneProduct denotes Hp NCBIGene:3240
7242 1107-1109 DiseaseOrPhenotypicFeature denotes DM MESH:D003920
7243 1127-1136 ChemicalEntity denotes vitamin E MESH:D014810
7244 1249-1251 GeneOrGeneProduct denotes Hp NCBIGene:3240
7245 1265-1274 ChemicalEntity denotes vitamin E MESH:D014810
7246 1320-1322 GeneOrGeneProduct denotes Hp NCBIGene:3240
7247 1336-1338 DiseaseOrPhenotypicFeature denotes DM MESH:D003920
7248 1379-1381 GeneOrGeneProduct denotes Hp NCBIGene:3240
7249 1391-1400 ChemicalEntity denotes vitamin E MESH:D014810
7250 1415-1433 DiseaseOrPhenotypicFeature denotes myocardial infarct MESH:D009203
7251 1435-1441 DiseaseOrPhenotypicFeature denotes stroke MESH:D020521
7252 1445-1465 DiseaseOrPhenotypicFeature denotes cardiovascular death MESH:D002318
7253 1494-1503 ChemicalEntity denotes vitamin E MESH:D014810
7254 1507-1509 GeneOrGeneProduct denotes Hp NCBIGene:3240
7255 1514-1516 DiseaseOrPhenotypicFeature denotes DM MESH:D003920
7256 1655-1657 DiseaseOrPhenotypicFeature denotes DM MESH:D003920
7257 1678-1680 GeneOrGeneProduct denotes Hp NCBIGene:3240
7258 1714-1716 GeneOrGeneProduct denotes Hp NCBIGene:3240
7259 1726-1735 ChemicalEntity denotes vitamin E MESH:D014810

LitCoin_Mondo

Id Subject Object Predicate Lexical cue mondo_id
T1 18-40 DiseaseOrPhenotypicFeature denotes cardiovascular disease 0004995
T2 61-78 DiseaseOrPhenotypicFeature denotes diabetes mellitus 0005015
T3 141-158 DiseaseOrPhenotypicFeature denotes diabetes mellitus 0005015
T4 227-249 DiseaseOrPhenotypicFeature denotes cardiovascular disease 0004995
T5 690-711 DiseaseOrPhenotypicFeature denotes myocardial infarction 0005068
T6 1415-1433 DiseaseOrPhenotypicFeature denotes myocardial infarct 0005068

LitCoin-GeneOrGeneProduct-v0

Id Subject Object Predicate Lexical cue
T28 1249-1251 GeneOrGeneProduct denotes Hp
T29 1292-1295 GeneOrGeneProduct denotes end
T30 1296-1301 GeneOrGeneProduct denotes point
T31 1320-1322 GeneOrGeneProduct denotes Hp
T32 1379-1385 GeneOrGeneProduct denotes Hp 2-2
T33 1379-1381 GeneOrGeneProduct denotes Hp
T34 1507-1513 GeneOrGeneProduct denotes Hp 2-2
T35 1507-1509 GeneOrGeneProduct denotes Hp
T36 1596-1601 GeneOrGeneProduct denotes years
T37 1678-1680 GeneOrGeneProduct denotes Hp
T38 1714-1720 GeneOrGeneProduct denotes Hp 2-2
T39 1714-1716 GeneOrGeneProduct denotes Hp
T40 1750-1756 GeneOrGeneProduct denotes highly
T1 10-17 GeneOrGeneProduct denotes reduces
T2 61-69 GeneOrGeneProduct denotes diabetes
T3 87-98 GeneOrGeneProduct denotes haptoglobin
T4 141-149 GeneOrGeneProduct denotes diabetes
T5 172-183 GeneOrGeneProduct denotes Haptoglobin
T6 184-192 GeneOrGeneProduct denotes (Hp) 2-2
T7 185-187 GeneOrGeneProduct denotes Hp
T8 286-288 GeneOrGeneProduct denotes Hp
T9 291-300 GeneOrGeneProduct denotes 2 protein
T10 327-331 GeneOrGeneProduct denotes test
T11 449-455 GeneOrGeneProduct denotes Hp 2-2
T12 449-451 GeneOrGeneProduct denotes Hp
T13 484-491 GeneOrGeneProduct denotes METHODS
T14 496-510 GeneOrGeneProduct denotes determined the
T15 511-513 GeneOrGeneProduct denotes Hp
T16 559-563 GeneOrGeneProduct denotes HOPE
T17 568-573 GeneOrGeneProduct denotes ICARE
T18 615-617 GeneOrGeneProduct denotes Hp
T19 846-851 GeneOrGeneProduct denotes Based
T20 900-904 GeneOrGeneProduct denotes long
T21 905-909 GeneOrGeneProduct denotes term
T22 923-927 GeneOrGeneProduct denotes in a
T23 993-997 GeneOrGeneProduct denotes Meta
T24 1087-1090 GeneOrGeneProduct denotes end
T25 1091-1096 GeneOrGeneProduct denotes point
T26 1100-1106 GeneOrGeneProduct denotes Hp 2-2
T27 1100-1102 GeneOrGeneProduct denotes Hp

LitCoin-GeneOrGeneProduct-v2

Id Subject Object Predicate Lexical cue
T1 61-69 GeneOrGeneProduct denotes diabetes
T2 87-98 GeneOrGeneProduct denotes haptoglobin
T3 141-149 GeneOrGeneProduct denotes diabetes
T4 172-183 GeneOrGeneProduct denotes Haptoglobin
T5 185-187 GeneOrGeneProduct denotes Hp
T6 286-288 GeneOrGeneProduct denotes Hp
T7 291-300 GeneOrGeneProduct denotes 2 protein
T8 449-455 GeneOrGeneProduct denotes Hp 2-2
T9 449-451 GeneOrGeneProduct denotes Hp
T10 511-513 GeneOrGeneProduct denotes Hp
T11 615-617 GeneOrGeneProduct denotes Hp
T12 905-909 GeneOrGeneProduct denotes term
T13 993-997 GeneOrGeneProduct denotes Meta
T14 1100-1106 GeneOrGeneProduct denotes Hp 2-2
T15 1100-1102 GeneOrGeneProduct denotes Hp
T16 1249-1251 GeneOrGeneProduct denotes Hp
T17 1320-1322 GeneOrGeneProduct denotes Hp
T18 1379-1385 GeneOrGeneProduct denotes Hp 2-2
T19 1379-1381 GeneOrGeneProduct denotes Hp
T20 1507-1513 GeneOrGeneProduct denotes Hp 2-2
T21 1507-1509 GeneOrGeneProduct denotes Hp
T22 1678-1680 GeneOrGeneProduct denotes Hp
T23 1714-1720 GeneOrGeneProduct denotes Hp 2-2
T24 1714-1716 GeneOrGeneProduct denotes Hp

LitCoin-Disease-MeSH

Id Subject Object Predicate Lexical cue originalLabel
T1 18-40 DiseaseOrPhenotypicFeature denotes cardiovascular disease D002318
T2 61-78 DiseaseOrPhenotypicFeature denotes diabetes mellitus D003920
T3 141-158 DiseaseOrPhenotypicFeature denotes diabetes mellitus D003920
T4 160-162 DiseaseOrPhenotypicFeature denotes DM D003920
T5 227-249 DiseaseOrPhenotypicFeature denotes cardiovascular disease D002318
T6 456-458 DiseaseOrPhenotypicFeature denotes DM D003920
T7 526-528 DiseaseOrPhenotypicFeature denotes DM D003920
T8 682-688 DiseaseOrPhenotypicFeature denotes stroke D020521
T9 690-711 DiseaseOrPhenotypicFeature denotes myocardial infarction D009203
T10 731-736 DiseaseOrPhenotypicFeature denotes death D003643
T11 1107-1109 DiseaseOrPhenotypicFeature denotes DM D003920
T12 1336-1338 DiseaseOrPhenotypicFeature denotes DM D003920
T13 1415-1433 DiseaseOrPhenotypicFeature denotes myocardial infarct D009203
T14 1435-1441 DiseaseOrPhenotypicFeature denotes stroke D020521
T15 1460-1465 DiseaseOrPhenotypicFeature denotes death D003643
T16 1514-1516 DiseaseOrPhenotypicFeature denotes DM D003920
T17 1655-1657 DiseaseOrPhenotypicFeature denotes DM D003920

LitCoin_Mondo_095

Id Subject Object Predicate Lexical cue mondo_id
T1 18-40 DiseaseOrPhenotypicFeature denotes cardiovascular disease 0004995
T2 61-78 DiseaseOrPhenotypicFeature denotes diabetes mellitus 0005015
T3 141-158 DiseaseOrPhenotypicFeature denotes diabetes mellitus 0005015
T4 160-162 DiseaseOrPhenotypicFeature denotes DM 0016367|0005015
T6 185-187 DiseaseOrPhenotypicFeature denotes Hp 0008185
T7 227-249 DiseaseOrPhenotypicFeature denotes cardiovascular disease 0004995
T8 286-288 DiseaseOrPhenotypicFeature denotes Hp 0008185
T9 449-451 DiseaseOrPhenotypicFeature denotes Hp 0008185
T10 456-458 DiseaseOrPhenotypicFeature denotes DM 0016367|0005015
T12 511-513 DiseaseOrPhenotypicFeature denotes Hp 0008185
T13 526-528 DiseaseOrPhenotypicFeature denotes DM 0016367|0005015
T15 615-617 DiseaseOrPhenotypicFeature denotes Hp 0008185
T16 682-688 DiseaseOrPhenotypicFeature denotes stroke 0005098
T17 690-711 DiseaseOrPhenotypicFeature denotes myocardial infarction 0005068
T18 974-976 DiseaseOrPhenotypicFeature denotes CA 0004992
T19 1100-1102 DiseaseOrPhenotypicFeature denotes Hp 0008185
T20 1107-1109 DiseaseOrPhenotypicFeature denotes DM 0016367|0005015
T22 1249-1251 DiseaseOrPhenotypicFeature denotes Hp 0008185
T23 1320-1322 DiseaseOrPhenotypicFeature denotes Hp 0008185
T24 1336-1338 DiseaseOrPhenotypicFeature denotes DM 0016367|0005015
T26 1379-1381 DiseaseOrPhenotypicFeature denotes Hp 0008185
T27 1415-1433 DiseaseOrPhenotypicFeature denotes myocardial infarct 0005068
T28 1435-1441 DiseaseOrPhenotypicFeature denotes stroke 0005098
T29 1507-1509 DiseaseOrPhenotypicFeature denotes Hp 0008185
T30 1514-1516 DiseaseOrPhenotypicFeature denotes DM 0016367|0005015
T32 1655-1657 DiseaseOrPhenotypicFeature denotes DM 0016367|0005015
T34 1678-1680 DiseaseOrPhenotypicFeature denotes Hp 0008185
T35 1714-1716 DiseaseOrPhenotypicFeature denotes Hp 0008185

LitCoin-MeSH-Disease-2

Id Subject Object Predicate Lexical cue ID:
T1 18-40 DiseaseOrPhenotypicFeature denotes cardiovascular disease D002318
T2 61-78 DiseaseOrPhenotypicFeature denotes diabetes mellitus D003920
T3 141-158 DiseaseOrPhenotypicFeature denotes diabetes mellitus D003920
T4 160-162 DiseaseOrPhenotypicFeature denotes DM DISEASE|D003920
T6 227-249 DiseaseOrPhenotypicFeature denotes cardiovascular disease D002318
T7 456-458 DiseaseOrPhenotypicFeature denotes DM DISEASE|D003920
T9 526-528 DiseaseOrPhenotypicFeature denotes DM DISEASE|D003920
T11 682-688 DiseaseOrPhenotypicFeature denotes stroke DISEASE|D020521
T13 690-711 DiseaseOrPhenotypicFeature denotes myocardial infarction D009203
T14 731-736 DiseaseOrPhenotypicFeature denotes death D003643
T15 1107-1109 DiseaseOrPhenotypicFeature denotes DM DISEASE|D003920
T17 1336-1338 DiseaseOrPhenotypicFeature denotes DM DISEASE|D003920
T19 1415-1433 DiseaseOrPhenotypicFeature denotes myocardial infarct D009203
T20 1435-1459 DiseaseOrPhenotypicFeature denotes stroke or cardiovascular D009203
T21 1460-1465 DiseaseOrPhenotypicFeature denotes death D003643
T22 1514-1516 DiseaseOrPhenotypicFeature denotes DM DISEASE|D003920
T24 1655-1657 DiseaseOrPhenotypicFeature denotes DM DISEASE|D003920

LitCoin-MONDO_bioort2019

Id Subject Object Predicate Lexical cue #label
T1 18-40 DiseaseOrPhenotypicFeature denotes cardiovascular disease D002318
T2 61-78 DiseaseOrPhenotypicFeature denotes diabetes mellitus D003920
T3 141-158 DiseaseOrPhenotypicFeature denotes diabetes mellitus D003920
T4 160-162 DiseaseOrPhenotypicFeature denotes DM DISEASE|D003920
T6 227-249 DiseaseOrPhenotypicFeature denotes cardiovascular disease D002318
T7 456-458 DiseaseOrPhenotypicFeature denotes DM DISEASE|D003920
T9 526-528 DiseaseOrPhenotypicFeature denotes DM DISEASE|D003920
T11 682-688 DiseaseOrPhenotypicFeature denotes stroke D020521
T12 690-711 DiseaseOrPhenotypicFeature denotes myocardial infarction D009203
T13 1107-1109 DiseaseOrPhenotypicFeature denotes DM DISEASE|D003920
T15 1336-1338 DiseaseOrPhenotypicFeature denotes DM DISEASE|D003920
T17 1415-1433 DiseaseOrPhenotypicFeature denotes myocardial infarct D009203
T18 1435-1459 DiseaseOrPhenotypicFeature denotes stroke or cardiovascular D009203
T19 1514-1516 DiseaseOrPhenotypicFeature denotes DM DISEASE|D003920
T21 1655-1657 DiseaseOrPhenotypicFeature denotes DM DISEASE|D003920

LitCoin-Chemical-MeSH-CHEBI

Id Subject Object Predicate Lexical cue ID:
T1 0-9 ChemicalEntity denotes Vitamin E http://purl.obolibrary.org/obo/CHEBI_18145
T2 258-269 ChemicalEntity denotes antioxidant ChemicalEntity
T3 368-379 ChemicalEntity denotes antioxidant ChemicalEntity
T4 380-389 ChemicalEntity denotes vitamin E http://purl.obolibrary.org/obo/CHEBI_33234
T5 602-611 ChemicalEntity denotes vitamin E http://purl.obolibrary.org/obo/CHEBI_33234
T6 1127-1136 ChemicalEntity denotes vitamin E http://purl.obolibrary.org/obo/CHEBI_33234
T7 1265-1274 ChemicalEntity denotes vitamin E http://purl.obolibrary.org/obo/CHEBI_33234
T8 1391-1400 ChemicalEntity denotes vitamin E http://purl.obolibrary.org/obo/CHEBI_33234
T9 1494-1503 ChemicalEntity denotes vitamin E http://purl.obolibrary.org/obo/CHEBI_33234
T10 1726-1735 ChemicalEntity denotes vitamin E http://purl.obolibrary.org/obo/CHEBI_33234

LitCoin-NCBITaxon-2

Id Subject Object Predicate Lexical cue
T1 974-981 OrganismTaxon denotes CA, USA

LitCoin-GeneOrGeneProduct-v3

Id Subject Object Predicate Lexical cue
T1 87-98 GeneOrGeneProduct denotes haptoglobin
T2 172-183 GeneOrGeneProduct denotes Haptoglobin
T3 185-187 GeneOrGeneProduct denotes Hp
T4 286-288 GeneOrGeneProduct denotes Hp
T5 291-300 GeneOrGeneProduct denotes 2 protein
T6 449-455 GeneOrGeneProduct denotes Hp 2-2
T8 511-513 GeneOrGeneProduct denotes Hp
T9 615-617 GeneOrGeneProduct denotes Hp
T10 993-997 GeneOrGeneProduct denotes Meta
T11 1100-1106 GeneOrGeneProduct denotes Hp 2-2
T13 1249-1251 GeneOrGeneProduct denotes Hp
T14 1320-1322 GeneOrGeneProduct denotes Hp
T15 1379-1385 GeneOrGeneProduct denotes Hp 2-2
T17 1507-1513 GeneOrGeneProduct denotes Hp 2-2
T19 1678-1680 GeneOrGeneProduct denotes Hp
T20 1714-1720 GeneOrGeneProduct denotes Hp 2-2

LitCoin-training-merged

Id Subject Object Predicate Lexical cue #label ID:
T10 1726-1735 ChemicalEntity denotes vitamin E http://purl.obolibrary.org/obo/CHEBI_33234
T9 1494-1503 ChemicalEntity denotes vitamin E http://purl.obolibrary.org/obo/CHEBI_33234
T8 1391-1400 ChemicalEntity denotes vitamin E http://purl.obolibrary.org/obo/CHEBI_33234
T7 1265-1274 ChemicalEntity denotes vitamin E http://purl.obolibrary.org/obo/CHEBI_33234
T6 1127-1136 ChemicalEntity denotes vitamin E http://purl.obolibrary.org/obo/CHEBI_33234
T5 602-611 ChemicalEntity denotes vitamin E http://purl.obolibrary.org/obo/CHEBI_33234
T4 380-389 ChemicalEntity denotes vitamin E http://purl.obolibrary.org/obo/CHEBI_33234
T3 368-379 ChemicalEntity denotes antioxidant ChemicalEntity
T2 258-269 ChemicalEntity denotes antioxidant ChemicalEntity
T1 0-9 ChemicalEntity denotes Vitamin E http://purl.obolibrary.org/obo/CHEBI_18145
T20 1714-1720 GeneOrGeneProduct denotes Hp 2-2
T19 1678-1680 GeneOrGeneProduct denotes Hp
T17 1507-1513 GeneOrGeneProduct denotes Hp 2-2
T15 1379-1385 GeneOrGeneProduct denotes Hp 2-2
T14 1320-1322 GeneOrGeneProduct denotes Hp
T13 1249-1251 GeneOrGeneProduct denotes Hp
T11 1100-1106 GeneOrGeneProduct denotes Hp 2-2
T2217 993-997 GeneOrGeneProduct denotes Meta
T56400 615-617 GeneOrGeneProduct denotes Hp
T94636 511-513 GeneOrGeneProduct denotes Hp
T76828 449-455 GeneOrGeneProduct denotes Hp 2-2
T36156 291-300 GeneOrGeneProduct denotes 2 protein
T59346 286-288 GeneOrGeneProduct denotes Hp
T77087 185-187 GeneOrGeneProduct denotes Hp
T37501 172-183 GeneOrGeneProduct denotes Haptoglobin
T61156 87-98 GeneOrGeneProduct denotes haptoglobin
T21 1655-1657 DiseaseOrPhenotypicFeature denotes DM D003920|DISEASE
T69656 1514-1516 DiseaseOrPhenotypicFeature denotes DM D003920|DISEASE
T18 1435-1459 DiseaseOrPhenotypicFeature denotes stroke or cardiovascular D009203
T85235 1415-1433 DiseaseOrPhenotypicFeature denotes myocardial infarct D009203
T45530 1336-1338 DiseaseOrPhenotypicFeature denotes DM D003920|DISEASE
T21906 1107-1109 DiseaseOrPhenotypicFeature denotes DM D003920|DISEASE
T12 690-711 DiseaseOrPhenotypicFeature denotes myocardial infarction D009203
T43949 682-688 DiseaseOrPhenotypicFeature denotes stroke D020521
T34268 526-528 DiseaseOrPhenotypicFeature denotes DM D003920|DISEASE
T66958 456-458 DiseaseOrPhenotypicFeature denotes DM D003920|DISEASE
T10287 227-249 DiseaseOrPhenotypicFeature denotes cardiovascular disease D002318
T94888 160-162 DiseaseOrPhenotypicFeature denotes DM D003920|DISEASE
T96906 141-158 DiseaseOrPhenotypicFeature denotes diabetes mellitus D003920
T18649 61-78 DiseaseOrPhenotypicFeature denotes diabetes mellitus D003920
T32013 18-40 DiseaseOrPhenotypicFeature denotes cardiovascular disease D002318
T51231 974-981 OrganismTaxon denotes CA, USA

DisGeNET

Id Subject Object Predicate Lexical cue
T0 87-98 gene:3240 denotes haptoglobin
T1 61-78 disease:C0011849 denotes diabetes mellitus
T2 87-98 gene:3240 denotes haptoglobin
T3 18-40 disease:C0007222 denotes cardiovascular disease
T4 185-190 gene:283297 denotes Hp) 2
T5 227-249 disease:C0007222 denotes cardiovascular disease
T6 185-190 gene:283297 denotes Hp) 2
T7 141-162 disease:C0011849 denotes diabetes mellitus (DM
T8 172-183 gene:3240 denotes Haptoglobin
T9 227-249 disease:C0007222 denotes cardiovascular disease
T10 172-183 gene:3240 denotes Haptoglobin
T11 141-162 disease:C0011849 denotes diabetes mellitus (DM
T12 1379-1383 gene:283297 denotes Hp 2
T13 1415-1433 disease:C0027051 denotes myocardial infarct
R1 T0 T1 associated_with haptoglobin,diabetes mellitus
R2 T2 T3 associated_with haptoglobin,cardiovascular disease
R3 T4 T5 associated_with Hp) 2,cardiovascular disease
R4 T6 T7 associated_with Hp) 2,diabetes mellitus (DM
R5 T8 T9 associated_with Haptoglobin,cardiovascular disease
R6 T10 T11 associated_with Haptoglobin,diabetes mellitus (DM
R7 T12 T13 associated_with Hp 2,myocardial infarct

PubmedHPO

Id Subject Object Predicate Lexical cue
T1 141-158 HP_0000819 denotes diabetes mellitus

Allie

Id Subject Object Predicate Lexical cue
SS1_20415560_2_0 141-158 expanded denotes diabetes mellitus
SS2_20415560_2_0 160-162 abbr denotes DM
SS1_20415560_2_1 172-183 expanded denotes Haptoglobin
SS2_20415560_2_1 185-187 abbr denotes Hp
AE1_20415560_2_0 SS1_20415560_2_0 SS2_20415560_2_0 abbreviatedTo diabetes mellitus,DM
AE1_20415560_2_1 SS1_20415560_2_1 SS2_20415560_2_1 abbreviatedTo Haptoglobin,Hp

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
20415560-0#87#98#gene3240 87-98 gene3240 denotes haptoglobin
20415560-0#18#40#diseaseC0007222 18-40 diseaseC0007222 denotes cardiovascular disease
20415560-0#61#78#diseaseC0011849 61-78 diseaseC0011849 denotes diabetes mellitus
20415560-1#66#71#gene283297 185-190 gene283297 denotes Hp) 2
20415560-1#108#130#diseaseC0007222 227-249 diseaseC0007222 denotes cardiovascular disease
20415560-3#122#124#gene3240 615-617 gene3240 denotes Hp
20415560-3#189#195#diseaseC0038454 682-688 diseaseC0038454 denotes stroke
20415560-8#76#80#gene283297 1379-1383 gene283297 denotes Hp 2
20415560-8#112#130#diseaseC0027051 1415-1433 diseaseC0027051 denotes myocardial infarct
20415560-9#40#44#gene283297 1507-1511 gene283297 denotes Hp 2
20415560-9#47#49#diseaseC0011849 1514-1516 diseaseC0011849 denotes DM
87#98#gene324018#40#diseaseC0007222 20415560-0#87#98#gene3240 20415560-0#18#40#diseaseC0007222 associated_with haptoglobin,cardiovascular disease
87#98#gene324061#78#diseaseC0011849 20415560-0#87#98#gene3240 20415560-0#61#78#diseaseC0011849 associated_with haptoglobin,diabetes mellitus
66#71#gene283297108#130#diseaseC0007222 20415560-1#66#71#gene283297 20415560-1#108#130#diseaseC0007222 associated_with Hp) 2,cardiovascular disease
122#124#gene3240189#195#diseaseC0038454 20415560-3#122#124#gene3240 20415560-3#189#195#diseaseC0038454 associated_with Hp,stroke
76#80#gene283297112#130#diseaseC0027051 20415560-8#76#80#gene283297 20415560-8#112#130#diseaseC0027051 associated_with Hp 2,myocardial infarct
40#44#gene28329747#49#diseaseC0011849 20415560-9#40#44#gene283297 20415560-9#47#49#diseaseC0011849 associated_with Hp 2,DM