| Id |
Subject |
Object |
Predicate |
Lexical cue |
| T2 |
0-231 |
Sentence |
denotes |
A generalized deficiency of the mitochondrial enzyme, ornithine aminotransferase (OAT) is the inborn error in gyrate atrophy, an autosomal recessive degenerative disease of the choroid and retina of the eye that leads to blindness. |
| T2 |
0-231 |
Sentence |
denotes |
A generalized deficiency of the mitochondrial enzyme, ornithine aminotransferase (OAT) is the inborn error in gyrate atrophy, an autosomal recessive degenerative disease of the choroid and retina of the eye that leads to blindness. |
