| Id |
Subject |
Object |
Predicate |
Lexical cue |
| TextSentencer_T16 |
0-249 |
Sentence |
denotes |
Unlike the genotype/phenotype relationship seen for type I collagen defects and osteogenesis imperfecta, the null allele in this family appears to cause clinical features similar to those seen in cases with structural alterations in type V collagen. |
| T16 |
0-249 |
Sentence |
denotes |
Unlike the genotype/phenotype relationship seen for type I collagen defects and osteogenesis imperfecta, the null allele in this family appears to cause clinical features similar to those seen in cases with structural alterations in type V collagen. |
