| Id |
Subject |
Object |
Predicate |
Lexical cue |
| T1 |
14-18 |
GeneOrGeneProduct |
denotes |
MEN1 |
| T2 |
48-75 |
DiseaseOrPhenotypicFeature |
denotes |
primary hyperparathyroidism |
| T3 |
123-150 |
DiseaseOrPhenotypicFeature |
denotes |
Primary hyperparathyroidism |
| T4 |
152-156 |
DiseaseOrPhenotypicFeature |
denotes |
pHPT |
| T5 |
170-187 |
DiseaseOrPhenotypicFeature |
denotes |
endocrine disease |
| T6 |
267-286 |
DiseaseOrPhenotypicFeature |
denotes |
inherited disorders |
| T7 |
311-339 |
DiseaseOrPhenotypicFeature |
denotes |
multiple endocrine neoplasia |
| T8 |
341-351 |
DiseaseOrPhenotypicFeature |
denotes |
MEN1 and 2 |
| T9 |
375-379 |
GeneOrGeneProduct |
denotes |
MEN1 |
| T10 |
422-440 |
DiseaseOrPhenotypicFeature |
denotes |
parathyroid tumors |
| T11 |
499-503 |
GeneOrGeneProduct |
denotes |
MEN1 |
| T12 |
527-535 |
OrganismTaxon |
denotes |
patients |
| T13 |
575-579 |
DiseaseOrPhenotypicFeature |
denotes |
pHPT |
| T14 |
589-623 |
DiseaseOrPhenotypicFeature |
denotes |
parathyroid adenoma or hyperplasia |
| T15 |
634-643 |
DiseaseOrPhenotypicFeature |
denotes |
carcinoma |
| T16 |
724-732 |
ChemicalEntity |
denotes |
paraffin |
| T17 |
807-811 |
GeneOrGeneProduct |
denotes |
MEN1 |
| T18 |
826-830 |
GeneOrGeneProduct |
denotes |
MEN1 |
| T19 |
870-878 |
OrganismTaxon |
denotes |
patients |
| T20 |
886-911 |
DiseaseOrPhenotypicFeature |
denotes |
benign parathyroid lesion |
| T21 |
971-981 |
DiseaseOrPhenotypicFeature |
denotes |
carcinomas |
| T22 |
994-998 |
GeneOrGeneProduct |
denotes |
MEN1 |
| T23 |
1067-1074 |
SequenceVariant |
denotes |
222insT |
| T24 |
1110-1118 |
SequenceVariant |
denotes |
912delTA |
| T25 |
1152-1160 |
SequenceVariant |
denotes |
835del18 |
| T26 |
1197-1202 |
SequenceVariant |
denotes |
P291A |
| T27 |
1249-1253 |
SequenceVariant |
denotes |
L89R |
| T28 |
1290-1295 |
SequenceVariant |
denotes |
Q536X |
| T29 |
1398-1403 |
SequenceVariant |
denotes |
R171Q |
| T30 |
1423-1429 |
DiseaseOrPhenotypicFeature |
denotes |
tumors |
| T31 |
1440-1445 |
SequenceVariant |
denotes |
D418D |
| T32 |
1460-1467 |
SequenceVariant |
denotes |
GAC/GAT |
| T33 |
1491-1497 |
DiseaseOrPhenotypicFeature |
denotes |
tumors |
| T34 |
1719-1723 |
GeneOrGeneProduct |
denotes |
MEN1 |
| T35 |
1724-1729 |
DiseaseOrPhenotypicFeature |
denotes |
tumor |
| T36 |
1784-1802 |
DiseaseOrPhenotypicFeature |
denotes |
parathyroid tumors |
