| Id |
Subject |
Object |
Predicate |
Lexical cue |
db_id |
| 1495 |
21-26 |
SequenceVariant |
denotes |
L490R |
DBSNP:rs80338886 |
| 1496 |
31-36 |
SequenceVariant |
denotes |
V561X |
DBSNP:rs80338887 |
| 1497 |
45-67 |
GeneOrGeneProduct |
denotes |
transferrin receptor 2 |
NCBIGene:7036 |
| 1498 |
85-93 |
OrganismTaxon |
denotes |
patients |
NCBITaxon:9606 |
| 1499 |
99-114 |
DiseaseOrPhenotypicFeature |
denotes |
hemochromatosis |
MESH:D006432 |
| 1500 |
169-174 |
SequenceVariant |
denotes |
C282Y |
DBSNP:rs1800562 |
| 1501 |
191-194 |
GeneOrGeneProduct |
denotes |
HFE |
NCBIGene:3077 |
| 1502 |
246-261 |
DiseaseOrPhenotypicFeature |
denotes |
hemochromatosis |
MESH:D006432 |
| 1503 |
274-282 |
OrganismTaxon |
denotes |
patients |
NCBITaxon:9606 |
| 1504 |
339-347 |
OrganismTaxon |
denotes |
patients |
NCBITaxon:9606 |
| 1505 |
371-392 |
SequenceVariant |
denotes |
AVAQ 594-597 deletion |
p|DEL|594_597|AVAQ |
| 1506 |
400-420 |
GeneOrGeneProduct |
denotes |
transferrin receptor |
NCBIGene:7036 |
| 1507 |
422-426 |
GeneOrGeneProduct |
denotes |
TfR2 |
NCBIGene:7036 |
| 1508 |
457-461 |
GeneOrGeneProduct |
denotes |
TfR2 |
NCBIGene:7036 |
| 1509 |
482-497 |
DiseaseOrPhenotypicFeature |
denotes |
hemochromatosis |
MESH:D006432 |
| 1510 |
510-518 |
OrganismTaxon |
denotes |
patients |
NCBITaxon:9606 |
| 1511 |
545-553 |
OrganismTaxon |
denotes |
patients |
NCBITaxon:9606 |
| 1512 |
580-595 |
DiseaseOrPhenotypicFeature |
denotes |
hemochromatosis |
MESH:D006432 |
| 1513 |
704-707 |
GeneOrGeneProduct |
denotes |
HFE |
NCBIGene:3077 |
| 1514 |
712-716 |
GeneOrGeneProduct |
denotes |
TfR2 |
NCBIGene:7036 |
| 1515 |
829-832 |
GeneOrGeneProduct |
denotes |
HFE |
NCBIGene:3077 |
| 1516 |
846-850 |
GeneOrGeneProduct |
denotes |
TfR2 |
NCBIGene:7036 |
| 1517 |
876-884 |
SequenceVariant |
denotes |
1469T->G |
DBSNP:rs80338886 |
| 1518 |
886-891 |
SequenceVariant |
denotes |
L490R |
DBSNP:rs80338886 |
| 1519 |
897-905 |
SequenceVariant |
denotes |
1665delC |
DBSNP:rs80338887 |
| 1520 |
907-912 |
SequenceVariant |
denotes |
V561X |
DBSNP:rs80338887 |
| 1521 |
931-939 |
OrganismTaxon |
denotes |
patients |
NCBITaxon:9606 |
| 1522 |
960-964 |
SequenceVariant |
denotes |
714C |
DBSNP:rs34242818 |
| 1523 |
968-973 |
SequenceVariant |
denotes |
I238M |
DBSNP:rs34242818 |
| 1524 |
998-1005 |
OrganismTaxon |
denotes |
patient |
NCBITaxon:9606 |
| 1525 |
1011-1016 |
SequenceVariant |
denotes |
L490R |
DBSNP:rs80338886 |
| 1526 |
1022-1029 |
OrganismTaxon |
denotes |
patient |
NCBITaxon:9606 |
| 1527 |
1050-1055 |
SequenceVariant |
denotes |
L490R |
DBSNP:rs80338886 |
| 1528 |
1060-1065 |
SequenceVariant |
denotes |
I238M |
DBSNP:rs34242818 |
| 1529 |
1105-1120 |
DiseaseOrPhenotypicFeature |
denotes |
hemochromatosis |
MESH:D006432 |
| 1530 |
1159-1168 |
DiseaseOrPhenotypicFeature |
denotes |
cirrhotic |
MESH:D008103 |
| 1531 |
1186-1190 |
ChemicalEntity |
denotes |
iron |
MESH:D007501 |
| 1532 |
1220-1227 |
ChemicalEntity |
denotes |
glucose |
MESH:D005947 |
| 1533 |
1263-1280 |
DiseaseOrPhenotypicFeature |
denotes |
diabetes mellitus |
MESH:D003920 |
| 1534 |
1286-1293 |
OrganismTaxon |
denotes |
patient |
NCBITaxon:9606 |
| 1535 |
1309-1314 |
SequenceVariant |
denotes |
V561X |
DBSNP:rs80338887 |
| 1536 |
1326-1339 |
DiseaseOrPhenotypicFeature |
denotes |
iron overload |
MESH:D019190 |
| 1537 |
1358-1367 |
DiseaseOrPhenotypicFeature |
denotes |
cirrhosis |
MESH:D008103 |
| 1538 |
1369-1386 |
DiseaseOrPhenotypicFeature |
denotes |
diabetes mellitus |
MESH:D003920 |
| 1539 |
1391-1408 |
DiseaseOrPhenotypicFeature |
denotes |
skin pigmentation |
MESH:D010859 |
| 1540 |
1518-1526 |
OrganismTaxon |
denotes |
patients |
NCBITaxon:9606 |
| 1541 |
1532-1547 |
DiseaseOrPhenotypicFeature |
denotes |
hemochromatosis |
MESH:D006432 |
| 1542 |
1595-1599 |
GeneOrGeneProduct |
denotes |
TfR2 |
NCBIGene:7036 |
| 1543 |
1612-1616 |
GeneOrGeneProduct |
denotes |
TfR2 |
NCBIGene:7036 |
| 1544 |
1653-1668 |
DiseaseOrPhenotypicFeature |
denotes |
hemochromatosis |
MESH:D006432 |
