| Id |
Subject |
Object |
Predicate |
Lexical cue |
db_id |
| 7520 |
27-35 |
GeneOrGeneProduct |
denotes |
TSH-beta |
NCBIGene:7252 |
| 7521 |
60-93 |
DiseaseOrPhenotypicFeature |
denotes |
congenital central hypothyroidism |
MESH:D003409 |
| 7522 |
119-122 |
GeneOrGeneProduct |
denotes |
TSH |
NCBIGene:7252 |
| 7523 |
143-151 |
OrganismTaxon |
denotes |
Patients |
NCBITaxon:9606 |
| 7524 |
157-165 |
GeneOrGeneProduct |
denotes |
TSH-beta |
NCBIGene:7252 |
| 7525 |
186-211 |
DiseaseOrPhenotypicFeature |
denotes |
congenital hypothyroidism |
MESH:D003409 |
| 7526 |
226-229 |
GeneOrGeneProduct |
denotes |
TSH |
NCBIGene:7252 |
| 7527 |
395-403 |
GeneOrGeneProduct |
denotes |
TSH-beta |
NCBIGene:7252 |
| 7528 |
430-438 |
OrganismTaxon |
denotes |
patients |
NCBITaxon:9606 |
| 7529 |
444-477 |
DiseaseOrPhenotypicFeature |
denotes |
congenital central hypothyroidism |
MESH:D003409 |
| 7530 |
515-521 |
DiseaseOrPhenotypicFeature |
denotes |
anemia |
MESH:D000740 |
| 7531 |
532-539 |
OrganismTaxon |
denotes |
Patient |
NCBITaxon:9606 |
| 7532 |
559-565 |
SequenceVariant |
denotes |
G to A |
c|SUB|G||A |
| 7533 |
978-985 |
OrganismTaxon |
denotes |
patient |
NCBITaxon:9606 |
| 7534 |
1066-1073 |
SequenceVariant |
denotes |
313delT |
c|DEL|313|T |
| 7535 |
1075-1086 |
SequenceVariant |
denotes |
C105Vfs114X |
p|FS|C|105|V|114 |
| 7536 |
1153-1192 |
SequenceVariant |
denotes |
G for A at cDNA nucleotide position 323 |
c|SUB|G|323|A |
| 7537 |
1209-1213 |
SequenceVariant |
denotes |
C88Y |
p|SUB|C|88|Y |
| 7538 |
1299-1333 |
GeneOrGeneProduct |
denotes |
glycoprotein hormone-beta subunits |
NCBIGene:122876 |
| 7539 |
1383-1387 |
SequenceVariant |
denotes |
C88Y |
p|SUB|C|88|Y |
| 7540 |
1519-1523 |
SequenceVariant |
denotes |
C88Y |
p|SUB|C|88|Y |
| 7541 |
1580-1594 |
DiseaseOrPhenotypicFeature |
denotes |
TSH deficiency |
MESH:D007037 |
| 7542 |
1656-1685 |
DiseaseOrPhenotypicFeature |
denotes |
isolated pituitary deficiency |
MESH:C566321 |
| 7543 |
1760-1782 |
DiseaseOrPhenotypicFeature |
denotes |
central hypothyroidism |
MESH:D007037 |
| 7544 |
1833-1839 |
DiseaseOrPhenotypicFeature |
denotes |
anemia |
MESH:D000740 |