| Id |
Subject |
Object |
Predicate |
Lexical cue |
db_id |
| 7894 |
4-20 |
GeneOrGeneProduct |
denotes |
fibrinogen gamma |
NCBIGene:2266 |
| 7895 |
21-29 |
SequenceVariant |
denotes |
10034C>T |
DBSNP:rs2066865 |
| 7896 |
66-93 |
DiseaseOrPhenotypicFeature |
denotes |
Peripheral Arterial Disease |
MESH:D058729 |
| 7897 |
109-119 |
GeneOrGeneProduct |
denotes |
fibrinogen |
NCBIGene:2243|NCBIGene:2244|NCBIGene:2266 |
| 7898 |
123-129 |
GeneOrGeneProduct |
denotes |
fibrin |
NCBIGene:2243|NCBIGene:2244|NCBIGene:2266 |
| 7899 |
204-210 |
GeneOrGeneProduct |
denotes |
fibrin |
NCBIGene:2243|NCBIGene:2244|NCBIGene:2266 |
| 7900 |
217-227 |
GeneOrGeneProduct |
denotes |
Fibrinogen |
NCBIGene:2243|NCBIGene:2244|NCBIGene:2266 |
| 7901 |
317-333 |
GeneOrGeneProduct |
denotes |
fibrinogen alpha |
NCBIGene:2243 |
| 7902 |
335-338 |
GeneOrGeneProduct |
denotes |
FGA |
NCBIGene:2243 |
| 7903 |
341-356 |
GeneOrGeneProduct |
denotes |
fibrinogen beta |
NCBIGene:2244 |
| 7904 |
358-361 |
GeneOrGeneProduct |
denotes |
FGB |
NCBIGene:2244 |
| 7905 |
367-383 |
GeneOrGeneProduct |
denotes |
fibrinogen gamma |
NCBIGene:2266 |
| 7906 |
385-388 |
GeneOrGeneProduct |
denotes |
FGG |
NCBIGene:2266 |
| 7907 |
479-482 |
GeneOrGeneProduct |
denotes |
FGG |
NCBIGene:2266 |
| 7908 |
489-492 |
GeneOrGeneProduct |
denotes |
FGG |
NCBIGene:2266 |
| 7909 |
493-501 |
SequenceVariant |
denotes |
10034C>T |
DBSNP:rs2066865 |
| 7910 |
503-512 |
SequenceVariant |
denotes |
rs2066865 |
DBSNP:rs2066865 |
| 7911 |
539-561 |
DiseaseOrPhenotypicFeature |
denotes |
deep venous thrombosis |
MESH:D020246 |
| 7912 |
566-587 |
DiseaseOrPhenotypicFeature |
denotes |
myocardial infarction |
MESH:D009203 |
| 7913 |
662-689 |
DiseaseOrPhenotypicFeature |
denotes |
peripheral arterial disease |
MESH:D058729 |
| 7914 |
691-694 |
DiseaseOrPhenotypicFeature |
denotes |
PAD |
MESH:D058729 |
| 7915 |
756-764 |
OrganismTaxon |
denotes |
patients |
NCBITaxon:9606 |
| 7916 |
781-784 |
DiseaseOrPhenotypicFeature |
denotes |
PAD |
MESH:D058729 |
| 7917 |
811-814 |
GeneOrGeneProduct |
denotes |
FGG |
NCBIGene:2266 |
| 7918 |
873-876 |
GeneOrGeneProduct |
denotes |
FGG |
NCBIGene:2266 |
| 7919 |
939-942 |
DiseaseOrPhenotypicFeature |
denotes |
PAD |
MESH:D058729 |
| 7920 |
943-951 |
OrganismTaxon |
denotes |
patients |
NCBITaxon:9606 |
| 7921 |
1123-1131 |
DiseaseOrPhenotypicFeature |
denotes |
diabetes |
MESH:D003920 |
| 7922 |
1142-1154 |
DiseaseOrPhenotypicFeature |
denotes |
hypertension |
MESH:D006973 |
| 7923 |
1159-1179 |
DiseaseOrPhenotypicFeature |
denotes |
hypercholesterolemia |
MESH:D006937 |
| 7924 |
1185-1188 |
GeneOrGeneProduct |
denotes |
FGG |
NCBIGene:2266 |
| 7925 |
1189-1196 |
SequenceVariant |
denotes |
10034 T |
DBSNP:rs2066865 |
| 7926 |
1259-1262 |
DiseaseOrPhenotypicFeature |
denotes |
PAD |
MESH:D058729 |
| 7927 |
1333-1336 |
GeneOrGeneProduct |
denotes |
FGG |
NCBIGene:2266 |
| 7928 |
1337-1345 |
SequenceVariant |
denotes |
10034C>T |
DBSNP:rs2066865 |
| 7929 |
1411-1414 |
DiseaseOrPhenotypicFeature |
denotes |
PAD |
MESH:D058729 |
| 7930 |
1451-1454 |
GeneOrGeneProduct |
denotes |
FGG |
NCBIGene:2266 |
| 7931 |
1455-1462 |
SequenceVariant |
denotes |
10034 T |
DBSNP:rs2066865 |
| 7932 |
1529-1532 |
DiseaseOrPhenotypicFeature |
denotes |
PAD |
MESH:D058729 |
