| Id |
Subject |
Object |
Predicate |
Lexical cue |
db_id |
| 4289 |
66-74 |
OrganismTaxon |
denotes |
patients |
NCBITaxon:9606 |
| 4290 |
93-97 |
GeneOrGeneProduct |
denotes |
GJB2 |
NCBIGene:2706 |
| 4291 |
154-186 |
DiseaseOrPhenotypicFeature |
denotes |
sensorineural hearing impairment |
MESH:D034381 |
| 4292 |
405-423 |
DiseaseOrPhenotypicFeature |
denotes |
hearing impairment |
MESH:D034381 |
| 4293 |
461-465 |
GeneOrGeneProduct |
denotes |
GJB2 |
NCBIGene:2706 |
| 4294 |
516-520 |
GeneOrGeneProduct |
denotes |
GJB2 |
NCBIGene:2706 |
| 4295 |
527-535 |
OrganismTaxon |
denotes |
patients |
NCBITaxon:9606 |
| 4296 |
541-559 |
DiseaseOrPhenotypicFeature |
denotes |
hearing impairment |
MESH:D034381 |
| 4297 |
607-611 |
GeneOrGeneProduct |
denotes |
GJB6 |
NCBIGene:10804 |
| 4298 |
616-620 |
GeneOrGeneProduct |
denotes |
GJB3 |
NCBIGene:2707 |
| 4299 |
657-661 |
GeneOrGeneProduct |
denotes |
GJB2 |
NCBIGene:2706 |
| 4300 |
707-711 |
GeneOrGeneProduct |
denotes |
GJB2 |
NCBIGene:2706 |
| 4301 |
725-733 |
OrganismTaxon |
denotes |
patients |
NCBITaxon:9606 |
| 4302 |
776-784 |
SequenceVariant |
denotes |
-3170G>A |
c|SUB|G|-3170|A |
| 4303 |
808-812 |
GeneOrGeneProduct |
denotes |
GJB2 |
NCBIGene:2706 |
| 4304 |
834-842 |
OrganismTaxon |
denotes |
patients |
NCBITaxon:9606 |
| 4305 |
861-869 |
SequenceVariant |
denotes |
-3170G>A |
c|SUB|G|-3170|A |
| 4306 |
899-906 |
SequenceVariant |
denotes |
p.R127H |
DBSNP:rs111033196 |
| 4307 |
920-924 |
GeneOrGeneProduct |
denotes |
GJB2 |
NCBIGene:2706 |
| 4308 |
967-971 |
GeneOrGeneProduct |
denotes |
GJB6 |
NCBIGene:10804 |
| 4309 |
979-983 |
GeneOrGeneProduct |
denotes |
GJB6 |
NCBIGene:10804 |
| 4310 |
1047-1051 |
GeneOrGeneProduct |
denotes |
GJB3 |
NCBIGene:2707 |
| 4311 |
1053-1061 |
SequenceVariant |
denotes |
c.357C>T |
DBSNP:rs41310442 |
| 4312 |
1063-1071 |
SequenceVariant |
denotes |
c.798C>T |
DBSNP:rs35983826 |
| 4313 |
1076-1083 |
SequenceVariant |
denotes |
c.94C>T |
DBSNP:rs1805063 |
| 4314 |
1085-1091 |
SequenceVariant |
denotes |
p.R32W |
DBSNP:rs1805063 |
| 4315 |
1210-1218 |
SequenceVariant |
denotes |
-3170G>A |
c|SUB|G|-3170|A |
| 4316 |
1244-1252 |
SequenceVariant |
denotes |
c.35delG |
DBSNP:rs80338939 |
| 4317 |
1257-1265 |
OrganismTaxon |
denotes |
patients |
NCBITaxon:9606 |
| 4318 |
1271-1289 |
DiseaseOrPhenotypicFeature |
denotes |
hearing impairment |
MESH:D034381 |
