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PubMed:10482951 JSONTXT 11 Projects

Annnotations TAB TSV DIC JSON TextAE Lectin_function IAV-Glycan

Id Subject Object Predicate Lexical cue
TextSentencer_T1 0-169 Sentence denotes A previously unrecognised phenotype characterised by obesity, muscular hypotonia, and ability to speak in patients with Angelman syndrome caused by an imprinting defect.
T1 0-169 Sentence denotes A previously unrecognised phenotype characterised by obesity, muscular hypotonia, and ability to speak in patients with Angelman syndrome caused by an imprinting defect.
TextSentencer_T2 170-357 Sentence denotes The clinical features of Angelman syndrome (AS) comprise severe mental retardation, postnatal microcephaly, macrostomia and prognathia, absence of speech, ataxia, and a happy disposition.
T2 170-357 Sentence denotes The clinical features of Angelman syndrome (AS) comprise severe mental retardation, postnatal microcephaly, macrostomia and prognathia, absence of speech, ataxia, and a happy disposition.
TextSentencer_T3 358-494 Sentence denotes We report on seven patients who lack most of these features, but presented with obesity, muscular hypotonia and mild mental retardation.
T3 358-494 Sentence denotes We report on seven patients who lack most of these features, but presented with obesity, muscular hypotonia and mild mental retardation.
TextSentencer_T4 495-595 Sentence denotes Based on the latter findings, the patients were initially suspected of having Prader-Willi syndrome.
T4 495-595 Sentence denotes Based on the latter findings, the patients were initially suspected of having Prader-Willi syndrome.
TextSentencer_T5 596-716 Sentence denotes DNA methylation analysis of SNRPN and D15S63, however, revealed an AS pattern, ie the maternal band was faint or absent.
T5 596-716 Sentence denotes DNA methylation analysis of SNRPN and D15S63, however, revealed an AS pattern, ie the maternal band was faint or absent.
TextSentencer_T6 717-837 Sentence denotes Cytogenetic studies and microsatellite analysis demonstrated apparently normal chromosomes 15 of biparental inheritance.
T6 717-837 Sentence denotes Cytogenetic studies and microsatellite analysis demonstrated apparently normal chromosomes 15 of biparental inheritance.
TextSentencer_T7 838-937 Sentence denotes We conclude that these patients have an imprinting defect and a previously unrecognised form of AS.
T7 838-937 Sentence denotes We conclude that these patients have an imprinting defect and a previously unrecognised form of AS.
TextSentencer_T8 938-1034 Sentence denotes The mild phenotype may be explained by an incomplete imprinting defect or by cellular mosaicism.
T8 938-1034 Sentence denotes The mild phenotype may be explained by an incomplete imprinting defect or by cellular mosaicism.