| Id |
Subject |
Object |
Predicate |
Lexical cue |
db_id |
| 698 |
24-26 |
GeneOrGeneProduct |
denotes |
F5 |
NCBIGene:2153 |
| 699 |
58-99 |
DiseaseOrPhenotypicFeature |
denotes |
inherited coagulation factor V deficiency |
MESH:D005166 |
| 700 |
193-227 |
DiseaseOrPhenotypicFeature |
denotes |
inherited factor V (FV) deficiency |
MESH:D005166 |
| 701 |
314-349 |
DiseaseOrPhenotypicFeature |
denotes |
inherited coagulation FV deficiency |
MESH:D005166 |
| 702 |
387-389 |
GeneOrGeneProduct |
denotes |
FV |
NCBIGene:2153 |
| 703 |
456-458 |
GeneOrGeneProduct |
denotes |
F5 |
NCBIGene:2153 |
| 704 |
712-722 |
SequenceVariant |
denotes |
IVS8 -2A>G |
c|SUB|A|IVS8-2|G |
| 705 |
745-747 |
GeneOrGeneProduct |
denotes |
F5 |
NCBIGene:2153 |
| 706 |
952-1001 |
SequenceVariant |
denotes |
insertion introduced eight additional amino acids |
p|INS||8 |
| 707 |
1016-1018 |
GeneOrGeneProduct |
denotes |
FV |
NCBIGene:2153 |
| 708 |
1058-1060 |
GeneOrGeneProduct |
denotes |
F5 |
NCBIGene:2153 |
| 709 |
1100-1112 |
SequenceVariant |
denotes |
2238-9del AG |
c|DEL|2238_2239|AG |
| 710 |
1167-1173 |
SequenceVariant |
denotes |
689 AA |
c|Allele|A|689 |
| 711 |
1198-1208 |
SequenceVariant |
denotes |
G6410 by T |
g|SUB|G|6410|T |
| 712 |
1250-1260 |
SequenceVariant |
denotes |
Gly2079Val |
p|SUB|G|2079|V |
| 713 |
1268-1270 |
GeneOrGeneProduct |
denotes |
F5 |
NCBIGene:2153 |
| 714 |
1287-1297 |
SequenceVariant |
denotes |
IVS8 -2A>G |
c|SUB|A|IVS8-2|G |
| 715 |
1299-1311 |
SequenceVariant |
denotes |
2238-9del AG |
c|DEL|2238_2239|AG |
| 716 |
1316-1322 |
SequenceVariant |
denotes |
G6410T |
g|SUB|G|6410|T |
| 717 |
1374-1398 |
DiseaseOrPhenotypicFeature |
denotes |
congenital FV deficiency |
MESH:D005166 |
