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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
1302032-0#0#18#diseaseC0016667 52-145 diseaseC0016667 denotes FMR1 deletion. We describe a patient with typical clinical features of the fragile X syndrome
1302032-0#52#56#gene2332 638-642 gene2332 denotes FMR1
52#56#gene23320#18#diseaseC0016667 1302032-0#52#56#gene2332 1302032-0#0#18#diseaseC0016667 associated_with FMR1,"FMR1 deletion. We describe a patient with typical clinical features of the fragile X syndrome"