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PubMed:10915770 JSONTXT 11 Projects

Annnotations TAB TSV DIC JSON TextAE Lectin_function IAV-Glycan

Id Subject Object Predicate Lexical cue
10915770-0#29#35#gene54551 29-35 gene54551 denotes MAGEL2
10915770-0#54#75#diseaseC0032897 54-75 diseaseC0032897 denotes Prader-willi syndrome
10915770-9#38#44#gene4692 1509-1515 gene4692 denotes necdin
10915770-9#105#108#diseaseC0032897 1576-1579 diseaseC0032897 denotes PWS
10915770-9#118#124#gene54551 1589-1595 gene54551 denotes MAGEL2
10915770-9#183#202#diseaseC0432072 1654-1673 diseaseC0432072 denotes dysmorphic features
10915770-9#183#202#diseaseC0432072 1654-1673 diseaseC0432072 denotes dysmorphic features
10915770-9#223#226#diseaseC0032897 1694-1697 diseaseC0032897 denotes PWS
118#124#gene54551105#108#diseaseC0032897 10915770-9#118#124#gene54551 10915770-9#105#108#diseaseC0032897 associated_with MAGEL2,PWS
118#124#gene54551183#202#diseaseC0432072 10915770-9#118#124#gene54551 10915770-9#183#202#diseaseC0432072 associated_with MAGEL2,dysmorphic features
118#124#gene54551183#202#diseaseC0432072 10915770-9#118#124#gene54551 10915770-9#183#202#diseaseC0432072 associated_with MAGEL2,dysmorphic features
118#124#gene54551223#226#diseaseC0032897 10915770-9#118#124#gene54551 10915770-9#223#226#diseaseC0032897 associated_with MAGEL2,PWS
29#35#gene5455154#75#diseaseC0032897 10915770-0#29#35#gene54551 10915770-0#54#75#diseaseC0032897 associated_with MAGEL2,Prader-willi syndrome
38#44#gene4692105#108#diseaseC0032897 10915770-9#38#44#gene4692 10915770-9#105#108#diseaseC0032897 associated_with necdin,PWS
38#44#gene4692183#202#diseaseC0432072 10915770-9#38#44#gene4692 10915770-9#183#202#diseaseC0432072 associated_with necdin,dysmorphic features
38#44#gene4692183#202#diseaseC0432072 10915770-9#38#44#gene4692 10915770-9#183#202#diseaseC0432072 associated_with necdin,dysmorphic features
38#44#gene4692223#226#diseaseC0032897 10915770-9#38#44#gene4692 10915770-9#223#226#diseaseC0032897 associated_with necdin,PWS