| Id |
Subject |
Object |
Predicate |
Lexical cue |
db_id |
| 7986 |
22-26 |
ChemicalEntity |
denotes |
iron |
MESH:D007501 |
| 7987 |
50-61 |
ChemicalEntity |
denotes |
deferasirox |
MESH:D000077588 |
| 7988 |
65-83 |
DiseaseOrPhenotypicFeature |
denotes |
aceruloplasminemia |
MESH:C536004 |
| 7989 |
133-151 |
DiseaseOrPhenotypicFeature |
denotes |
Aceruloplasminemia |
MESH:C536004 |
| 7990 |
162-207 |
DiseaseOrPhenotypicFeature |
denotes |
autosomal recessive neurodegenerative disease |
MESH:D020271 |
| 7991 |
240-244 |
ChemicalEntity |
denotes |
iron |
MESH:D007501 |
| 7992 |
288-306 |
DiseaseOrPhenotypicFeature |
denotes |
movement disorders |
MESH:D009069 |
| 7993 |
308-328 |
DiseaseOrPhenotypicFeature |
denotes |
retinal degeneration |
MESH:D012162 |
| 7994 |
334-351 |
DiseaseOrPhenotypicFeature |
denotes |
diabetes mellitus |
MESH:D003920 |
| 7995 |
353-366 |
GeneOrGeneProduct |
denotes |
Ceruloplasmin |
NCBIGene:1356 |
| 7996 |
385-396 |
ChemicalEntity |
denotes |
ferroxidase |
|
| 7997 |
451-455 |
ChemicalEntity |
denotes |
iron |
MESH:D007501 |
| 7998 |
467-471 |
ChemicalEntity |
denotes |
iron |
MESH:D007501 |
| 7999 |
483-494 |
GeneOrGeneProduct |
denotes |
transferrin |
NCBIGene:7018 |
| 8000 |
524-537 |
GeneOrGeneProduct |
denotes |
ceruloplasmin |
NCBIGene:1356 |
| 8001 |
553-564 |
SequenceVariant |
denotes |
c.2554+1G>T |
c|SUB|G|2554+1|T |
| 8002 |
597-615 |
DiseaseOrPhenotypicFeature |
denotes |
aceruloplasminemia |
MESH:C536004 |
| 8003 |
672-690 |
DiseaseOrPhenotypicFeature |
denotes |
movement disorders |
MESH:D009069 |
| 8004 |
695-703 |
DiseaseOrPhenotypicFeature |
denotes |
diabetes |
MESH:D003920 |
| 8005 |
791-822 |
SequenceVariant |
denotes |
deletion of amino acids 809-852 |
c|DEL|809_852| |
| 8006 |
920-928 |
OrganismTaxon |
denotes |
patients |
NCBITaxon:9606 |
| 8007 |
984-1002 |
DiseaseOrPhenotypicFeature |
denotes |
Aceruloplasminemia |
MESH:C536004 |
| 8008 |
1046-1059 |
DiseaseOrPhenotypicFeature |
denotes |
iron overload |
MESH:D019190 |
| 8009 |
1098-1102 |
ChemicalEntity |
denotes |
iron |
MESH:D007501 |
| 8010 |
1111-1119 |
GeneOrGeneProduct |
denotes |
hepcidin |
NCBIGene:57817 |
| 8011 |
1166-1179 |
DiseaseOrPhenotypicFeature |
denotes |
iron overload |
MESH:D019190 |
| 8012 |
1189-1193 |
ChemicalEntity |
denotes |
iron |
MESH:D007501 |
| 8013 |
1242-1246 |
ChemicalEntity |
denotes |
iron |
MESH:D007501 |
| 8014 |
1270-1281 |
ChemicalEntity |
denotes |
deferasirox |
MESH:D000077588 |
| 8015 |
1322-1329 |
GeneOrGeneProduct |
denotes |
insulin |
NCBIGene:3630 |
| 8016 |
1442-1455 |
DiseaseOrPhenotypicFeature |
denotes |
iron overload |
MESH:D019190 |
| 8017 |
1470-1488 |
DiseaseOrPhenotypicFeature |
denotes |
Aceruloplasminemia |
MESH:C536004 |
| 8018 |
1566-1570 |
ChemicalEntity |
denotes |
iron |
MESH:D007501 |
| 8019 |
1615-1619 |
ChemicalEntity |
denotes |
Iron |
MESH:D007501 |
| 8020 |
1636-1654 |
DiseaseOrPhenotypicFeature |
denotes |
aceruloplasminemia |
MESH:C536004 |
| 8021 |
1689-1693 |
ChemicalEntity |
denotes |
iron |
MESH:D007501 |
| 8022 |
1708-1716 |
GeneOrGeneProduct |
denotes |
hepcidin |
NCBIGene:57817 |
| 8023 |
1761-1774 |
DiseaseOrPhenotypicFeature |
denotes |
iron overload |
MESH:D019190 |
| 8024 |
1776-1780 |
ChemicalEntity |
denotes |
Iron |
MESH:D007501 |
| 8025 |
1796-1807 |
ChemicalEntity |
denotes |
deferasirox |
MESH:D000077588 |
| 8026 |
1844-1848 |
ChemicalEntity |
denotes |
iron |
MESH:D007501 |
| 8027 |
1876-1880 |
ChemicalEntity |
denotes |
iron |
MESH:D007501 |
