| Id |
Subject |
Object |
Predicate |
Lexical cue |
db_id |
| 4684 |
21-27 |
GeneOrGeneProduct |
denotes |
CHRNA1 |
NCBIGene:1134 |
| 4685 |
29-35 |
GeneOrGeneProduct |
denotes |
CHRNB1 |
NCBIGene:1140 |
| 4686 |
37-42 |
GeneOrGeneProduct |
denotes |
CHRND |
NCBIGene:1144 |
| 4687 |
48-53 |
GeneOrGeneProduct |
denotes |
RAPSN |
NCBIGene:5913 |
| 4688 |
63-90 |
DiseaseOrPhenotypicFeature |
denotes |
multiple pterygium syndrome |
MESH:C537377 |
| 4689 |
91-105 |
DiseaseOrPhenotypicFeature |
denotes |
fetal akinesia |
MESH:C536647 |
| 4690 |
106-114 |
OrganismTaxon |
denotes |
patients |
NCBITaxon:9606 |
| 4691 |
116-144 |
DiseaseOrPhenotypicFeature |
denotes |
Multiple pterygium syndromes |
MESH:C537377 |
| 4692 |
146-149 |
DiseaseOrPhenotypicFeature |
denotes |
MPS |
MESH:C537377 |
| 4693 |
180-208 |
DiseaseOrPhenotypicFeature |
denotes |
congenital anomaly disorders |
MESH:D000013 |
| 4694 |
283-301 |
DiseaseOrPhenotypicFeature |
denotes |
joint contractures |
MESH:D003286 |
| 4695 |
303-317 |
DiseaseOrPhenotypicFeature |
denotes |
arthrogryposis |
MESH:D001176 |
| 4696 |
320-323 |
DiseaseOrPhenotypicFeature |
denotes |
MPS |
MESH:C537377 |
| 4697 |
524-566 |
GeneOrGeneProduct |
denotes |
embryonal acetylcholine receptor g subunit |
NCBIGene:1146 |
| 4698 |
568-573 |
GeneOrGeneProduct |
denotes |
CHRNG |
NCBIGene:1146 |
| 4699 |
611-614 |
DiseaseOrPhenotypicFeature |
denotes |
MPS |
MESH:C537377 |
| 4700 |
663-677 |
DiseaseOrPhenotypicFeature |
denotes |
fetal akinesia |
MESH:C536647 |
| 4701 |
773-776 |
DiseaseOrPhenotypicFeature |
denotes |
MPS |
MESH:C537377 |
| 4702 |
777-791 |
DiseaseOrPhenotypicFeature |
denotes |
fetal akinesia |
MESH:C536647 |
| 4703 |
840-843 |
DiseaseOrPhenotypicFeature |
denotes |
MPS |
MESH:C537377 |
| 4704 |
844-858 |
DiseaseOrPhenotypicFeature |
denotes |
fetal akinesia |
MESH:C536647 |
| 4705 |
867-872 |
GeneOrGeneProduct |
denotes |
CHRNG |
NCBIGene:1146 |
| 4706 |
904-910 |
GeneOrGeneProduct |
denotes |
CHRNA1 |
NCBIGene:1134 |
| 4707 |
912-918 |
GeneOrGeneProduct |
denotes |
CHRNB1 |
NCBIGene:1140 |
| 4708 |
920-925 |
GeneOrGeneProduct |
denotes |
CHRND |
NCBIGene:1144 |
| 4709 |
931-937 |
GeneOrGeneProduct |
denotes |
rapsyn |
NCBIGene:5913 |
| 4710 |
939-944 |
GeneOrGeneProduct |
denotes |
RAPSN |
NCBIGene:5913 |
| 4711 |
956-962 |
GeneOrGeneProduct |
denotes |
CHRNA1 |
NCBIGene:1134 |
| 4712 |
964-970 |
GeneOrGeneProduct |
denotes |
CHRNB1 |
NCBIGene:1140 |
| 4713 |
975-980 |
GeneOrGeneProduct |
denotes |
CHRND |
NCBIGene:1144 |
| 4714 |
1023-1028 |
GeneOrGeneProduct |
denotes |
RAPSN |
NCBIGene:5913 |
| 4715 |
1050-1066 |
SequenceVariant |
denotes |
c.1177-1178delAA |
c|DEL|1177_1178|AA |
| 4716 |
1136-1159 |
DiseaseOrPhenotypicFeature |
denotes |
fetal akinesia sequence |
MESH:C536647 |
| 4717 |
1173-1178 |
GeneOrGeneProduct |
denotes |
RAPSN |
NCBIGene:5913 |
| 4718 |
1211-1232 |
DiseaseOrPhenotypicFeature |
denotes |
congenital myasthenia |
MESH:D020294 |
| 4719 |
1321-1327 |
GeneOrGeneProduct |
denotes |
rapsyn |
NCBIGene:5913 |
| 4720 |
1347-1368 |
DiseaseOrPhenotypicFeature |
denotes |
congenital myasthenia |
MESH:D020294 |
| 4721 |
1422-1436 |
DiseaseOrPhenotypicFeature |
denotes |
fetal akinesia |
MESH:C536647 |
