| Id |
Subject |
Object |
Predicate |
Lexical cue |
| TextSentencer_T12 |
0-248 |
Sentence |
denotes |
A novel heterozygous mutation in exon 18 of the CYLD gene (c.2449delT) was identified, with a deletion of one nucleotide resulting in a premature translational termination codon at amino acid position 831 on the affected allele (p.Cys817Valfs X15). |
| T12 |
0-248 |
Sentence |
denotes |
A novel heterozygous mutation in exon 18 of the CYLD gene (c.2449delT) was identified, with a deletion of one nucleotide resulting in a premature translational termination codon at amino acid position 831 on the affected allele (p.Cys817Valfs X15). |
