| Id |
Subject |
Object |
Predicate |
Lexical cue |
| T1 |
0-25 |
DiseaseOrPhenotypicFeature |
denotes |
Congenital hypothyroidism |
| T2 |
55-78 |
GeneOrGeneProduct |
denotes |
sodium/iodide symporter |
| T3 |
99-122 |
DiseaseOrPhenotypicFeature |
denotes |
Iodide transport defect |
| T4 |
124-127 |
DiseaseOrPhenotypicFeature |
denotes |
ITD |
| T5 |
168-192 |
DiseaseOrPhenotypicFeature |
denotes |
inability of the thyroid |
| T6 |
208-214 |
ChemicalEntity |
denotes |
iodide |
| T7 |
307-332 |
DiseaseOrPhenotypicFeature |
denotes |
congenital hypothyroidism |
| T8 |
471-494 |
GeneOrGeneProduct |
denotes |
sodium/iodide symporter |
| T9 |
496-499 |
GeneOrGeneProduct |
denotes |
NIS |
| T10 |
502-509 |
OrganismTaxon |
denotes |
PATIENT |
| T11 |
525-530 |
OrganismTaxon |
denotes |
woman |
| T12 |
536-550 |
DiseaseOrPhenotypicFeature |
denotes |
hypothyroidism |
| T13 |
605-608 |
DiseaseOrPhenotypicFeature |
denotes |
ITD |
| T14 |
634-648 |
DiseaseOrPhenotypicFeature |
denotes |
nodular goitre |
| T15 |
668-674 |
ChemicalEntity |
denotes |
iodide |
| T16 |
733-739 |
ChemicalEntity |
denotes |
iodide |
| T17 |
764-778 |
DiseaseOrPhenotypicFeature |
denotes |
hypothyroidism |
| T18 |
825-836 |
ChemicalEntity |
denotes |
L-thyroxine |
| T19 |
872-883 |
ChemicalEntity |
denotes |
radioiodide |
| T20 |
968-973 |
OrganismTaxon |
denotes |
human |
| T21 |
974-977 |
GeneOrGeneProduct |
denotes |
TSH |
| T22 |
1000-1002 |
ChemicalEntity |
denotes |
I- |
| T23 |
1083-1085 |
ChemicalEntity |
denotes |
I- |
| T24 |
1152-1159 |
OrganismTaxon |
denotes |
patient |
| T25 |
1162-1165 |
GeneOrGeneProduct |
denotes |
NIS |
| T26 |
1201-1258 |
SequenceVariant |
denotes |
deletion of the coding sequence (nt 1314 through nt 1328) |
| T27 |
1267-1310 |
SequenceVariant |
denotes |
insertion of 15 nt duplicating the first 15 |
| T28 |
1342-1349 |
OrganismTaxon |
denotes |
patient |
| T29 |
1498-1556 |
SequenceVariant |
denotes |
lacking the five terminal amino acids of exon XI (439-443) |
| T30 |
1606-1611 |
CellLine |
denotes |
COS-7 |
| T31 |
1666-1679 |
SequenceVariant |
denotes |
del-(439-443) |
| T32 |
1680-1683 |
GeneOrGeneProduct |
denotes |
NIS |
| T33 |
1706-1712 |
ChemicalEntity |
denotes |
iodide |
| T34 |
1771-1774 |
DiseaseOrPhenotypicFeature |
denotes |
ITD |
| T35 |
1783-1790 |
OrganismTaxon |
denotes |
patient |
| T36 |
1856-1881 |
DiseaseOrPhenotypicFeature |
denotes |
congenital hypothyroidism |
| T37 |
1911-1914 |
GeneOrGeneProduct |
denotes |
NIS |
