PubMed:16440883 / 0-153 6 Projects
Annnotations
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
TextSentencer_T1 | 0-98 | Sentence | denotes | Apert syndrome with preaxial polydactyly showing the typical mutation Ser252Trp in the FGFR2 gene. |
T1 | 0-98 | Sentence | denotes | Apert syndrome with preaxial polydactyly showing the typical mutation Ser252Trp in the FGFR2 gene. |