| Id |
Subject |
Object |
Predicate |
Lexical cue |
| T1 |
22-26 |
ChemicalEntity |
denotes |
iron |
| T2 |
50-61 |
ChemicalEntity |
denotes |
deferasirox |
| T3 |
65-83 |
DiseaseOrPhenotypicFeature |
denotes |
aceruloplasminemia |
| T4 |
133-151 |
DiseaseOrPhenotypicFeature |
denotes |
Aceruloplasminemia |
| T5 |
162-207 |
DiseaseOrPhenotypicFeature |
denotes |
autosomal recessive neurodegenerative disease |
| T6 |
240-244 |
ChemicalEntity |
denotes |
iron |
| T7 |
288-306 |
DiseaseOrPhenotypicFeature |
denotes |
movement disorders |
| T8 |
308-328 |
DiseaseOrPhenotypicFeature |
denotes |
retinal degeneration |
| T9 |
334-351 |
DiseaseOrPhenotypicFeature |
denotes |
diabetes mellitus |
| T10 |
353-366 |
GeneOrGeneProduct |
denotes |
Ceruloplasmin |
| T11 |
385-396 |
ChemicalEntity |
denotes |
ferroxidase |
| T12 |
451-455 |
ChemicalEntity |
denotes |
iron |
| T13 |
467-471 |
ChemicalEntity |
denotes |
iron |
| T14 |
483-494 |
GeneOrGeneProduct |
denotes |
transferrin |
| T15 |
524-537 |
GeneOrGeneProduct |
denotes |
ceruloplasmin |
| T16 |
553-564 |
SequenceVariant |
denotes |
c.2554+1G>T |
| T17 |
597-615 |
DiseaseOrPhenotypicFeature |
denotes |
aceruloplasminemia |
| T18 |
672-690 |
DiseaseOrPhenotypicFeature |
denotes |
movement disorders |
| T19 |
695-703 |
DiseaseOrPhenotypicFeature |
denotes |
diabetes |
| T20 |
791-822 |
SequenceVariant |
denotes |
deletion of amino acids 809-852 |
| T21 |
920-928 |
OrganismTaxon |
denotes |
patients |
| T22 |
984-1002 |
DiseaseOrPhenotypicFeature |
denotes |
Aceruloplasminemia |
| T23 |
1046-1059 |
DiseaseOrPhenotypicFeature |
denotes |
iron overload |
| T24 |
1098-1102 |
ChemicalEntity |
denotes |
iron |
| T25 |
1111-1119 |
GeneOrGeneProduct |
denotes |
hepcidin |
| T26 |
1166-1179 |
DiseaseOrPhenotypicFeature |
denotes |
iron overload |
| T27 |
1189-1193 |
ChemicalEntity |
denotes |
iron |
| T28 |
1242-1246 |
ChemicalEntity |
denotes |
iron |
| T29 |
1270-1281 |
ChemicalEntity |
denotes |
deferasirox |
| T30 |
1322-1329 |
GeneOrGeneProduct |
denotes |
insulin |
| T31 |
1442-1455 |
DiseaseOrPhenotypicFeature |
denotes |
iron overload |
| T32 |
1470-1488 |
DiseaseOrPhenotypicFeature |
denotes |
Aceruloplasminemia |
| T33 |
1566-1570 |
ChemicalEntity |
denotes |
iron |
| T34 |
1615-1619 |
ChemicalEntity |
denotes |
Iron |
| T35 |
1636-1654 |
DiseaseOrPhenotypicFeature |
denotes |
aceruloplasminemia |
| T36 |
1689-1693 |
ChemicalEntity |
denotes |
iron |
| T37 |
1708-1716 |
GeneOrGeneProduct |
denotes |
hepcidin |
| T38 |
1761-1774 |
DiseaseOrPhenotypicFeature |
denotes |
iron overload |
| T39 |
1776-1780 |
ChemicalEntity |
denotes |
Iron |
| T40 |
1796-1807 |
ChemicalEntity |
denotes |
deferasirox |
| T41 |
1844-1848 |
ChemicalEntity |
denotes |
iron |
| T42 |
1876-1880 |
ChemicalEntity |
denotes |
iron |
