PubMed:25708779 JSONTXT 3 Projects

Annnotations TAB TSV DIC JSON TextAE Lectin_function IAV-Glycan

Id Subject Object Predicate Lexical cue
25708779-1#35#62#diseaseC1535926 188-215 diseaseC1535926 denotes neurodevelopmental disorder
25708779-1#106#111#gene4204 259-264 gene4204 denotes MECP2
25708779-1#133#163#diseaseC0036857 286-316 diseaseC0036857 denotes severe intellectual disability
25708779-1#189#197#diseaseC0004352 342-350 diseaseC0004352 denotes autistic
25708779-3#112#117#gene4204 565-570 gene4204 denotes MeCP2
25708779-3#188#191#diseaseC0035372 641-644 diseaseC0035372 denotes RTT
106#111#gene4204133#163#diseaseC0036857 25708779-1#106#111#gene4204 25708779-1#133#163#diseaseC0036857 associated_with MECP2,severe intellectual disability
106#111#gene4204189#197#diseaseC0004352 25708779-1#106#111#gene4204 25708779-1#189#197#diseaseC0004352 associated_with MECP2,autistic
106#111#gene420435#62#diseaseC1535926 25708779-1#106#111#gene4204 25708779-1#35#62#diseaseC1535926 associated_with MECP2,neurodevelopmental disorder
112#117#gene4204188#191#diseaseC0035372 25708779-3#112#117#gene4204 25708779-3#188#191#diseaseC0035372 associated_with MeCP2,RTT