| Id |
Subject |
Object |
Predicate |
Lexical cue |
| TextSentencer_T2 |
0-212 |
Sentence |
denotes |
Achondrogenesis type 1B is an autosomal recessive, lethal chondrodysplasia caused by mutations in the gene encoding a sulfate/chloride antiporter of the cell membrane (Superti-Furga, A., Hästbacka, J., Wilcox, W. |
| T2 |
0-212 |
Sentence |
denotes |
Achondrogenesis type 1B is an autosomal recessive, lethal chondrodysplasia caused by mutations in the gene encoding a sulfate/chloride antiporter of the cell membrane (Superti-Furga, A., Hästbacka, J., Wilcox, W. |
