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PubMed:8266996 JSONTXT 14 Projects

Annnotations TAB TSV DIC JSON TextAE Lectin_function IAV-Glycan

Id Subject Object Predicate Lexical cue
TextSentencer_T1 0-148 Sentence denotes Difference in methylation patterns within the D15S9 region of chromosome 15q11-13 in first cousins with Angelman syndrome and Prader-Willi syndrome.
T1 0-148 Sentence denotes Difference in methylation patterns within the D15S9 region of chromosome 15q11-13 in first cousins with Angelman syndrome and Prader-Willi syndrome.
TextSentencer_T2 149-268 Sentence denotes Abnormalities of chromosome region 15q11-13 are associated with Angelman syndrome (AS) and Prader-Willi syndrome (PWS).
T2 149-268 Sentence denotes Abnormalities of chromosome region 15q11-13 are associated with Angelman syndrome (AS) and Prader-Willi syndrome (PWS).
TextSentencer_T3 269-477 Sentence denotes Differences between the methylation patterns of the region of chromosome 15q11-13 which hybridizes to the highly conserved DNA, DN34, in normal individuals and in patients with AS and PWS have been described.
T3 269-477 Sentence denotes Differences between the methylation patterns of the region of chromosome 15q11-13 which hybridizes to the highly conserved DNA, DN34, in normal individuals and in patients with AS and PWS have been described.
TextSentencer_T4 478-611 Sentence denotes We report on a family in which first cousins are affected by AS and PWS as a result of a familial paracentric inversion of 15q11-q13.
T4 478-611 Sentence denotes We report on a family in which first cousins are affected by AS and PWS as a result of a familial paracentric inversion of 15q11-q13.
TextSentencer_T5 612-859 Sentence denotes The results of the studies on this family demonstrate the differences in the methylation patterns in the 2 conditions and the phenomenon of genomic imprinting, whereby genetic information is expressed differently dependent on the parent of origin.
T5 612-859 Sentence denotes The results of the studies on this family demonstrate the differences in the methylation patterns in the 2 conditions and the phenomenon of genomic imprinting, whereby genetic information is expressed differently dependent on the parent of origin.