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PubMed:1302032 JSONTXT 16 Projects

Annnotations TAB TSV DIC JSON TextAE Lectin_function IAV-Glycan

Id Subject Object Predicate Lexical cue
TextSentencer_T1 0-66 Sentence denotes Fragile X syndrome without CCG amplification has an FMR1 deletion.
T1 0-66 Sentence denotes Fragile X syndrome without CCG amplification has an FMR1 deletion.
TextSentencer_T2 67-249 Sentence denotes We describe a patient with typical clinical features of the fragile X syndrome, but without cytogenetic expression of the fragile X or an amplified CCG trinucleotide repeat fragment.
T2 67-249 Sentence denotes We describe a patient with typical clinical features of the fragile X syndrome, but without cytogenetic expression of the fragile X or an amplified CCG trinucleotide repeat fragment.
TextSentencer_T3 250-415 Sentence denotes The patient has a previously uncharacterized submicroscopic deletion encompassing the CCG repeat, the entire FMR1 gene and about 2.5 megabases of flanking sequences.
T3 250-415 Sentence denotes The patient has a previously uncharacterized submicroscopic deletion encompassing the CCG repeat, the entire FMR1 gene and about 2.5 megabases of flanking sequences.
TextSentencer_T4 416-643 Sentence denotes This finding confirms that the fragile X phenotype can exist, without amplification of the CCG repeat or cytogenetic expression of the fragile X, and that fragile X syndrome is a genetically homogeneous disorder involving FMR1.
T4 416-643 Sentence denotes This finding confirms that the fragile X phenotype can exist, without amplification of the CCG repeat or cytogenetic expression of the fragile X, and that fragile X syndrome is a genetically homogeneous disorder involving FMR1.
TextSentencer_T5 644-756 Sentence denotes We also found random X-inactivation in the mother of the patient who was shown to be a carrier of this deletion.
T5 644-756 Sentence denotes We also found random X-inactivation in the mother of the patient who was shown to be a carrier of this deletion.