PubMed:12369018 JSONTXT 5 Projects

Annnotations TAB TSV DIC JSON TextAE Lectin_function IAV-Glycan

Id Subject Object Predicate Lexical cue
12369018-0#44#49#gene10585 44-49 gene10585 denotes POMT1
12369018-0#74#101#diseaseC1837249 74-101 diseaseC1837249 denotes neuronal migration disorder
12369018-0#102#125#diseaseC0265221 102-125 diseaseC0265221 denotes Walker-Warburg syndrome
12369018-3#49#52#diseaseC0457133 501-504 diseaseC0457133 denotes MEB
12369018-3#54#61#gene55624 506-513 gene55624 denotes POMGnT1
12369018-8#62#66#diseaseC0410174 1049-1053 diseaseC0410174 denotes FCMD
12369018-8#71#74#gene55624 1058-1061 gene55624 denotes MEB
12369018-9#6#13#gene55624 1075-1082 gene55624 denotes POMGnT1
12369018-9#141#144#diseaseC0265221 1210-1213 diseaseC0265221 denotes WWS
44#49#gene10585102#125#diseaseC0265221 12369018-0#44#49#gene10585 12369018-0#102#125#diseaseC0265221 associated_with POMT1,Walker-Warburg syndrome
44#49#gene1058574#101#diseaseC1837249 12369018-0#44#49#gene10585 12369018-0#74#101#diseaseC1837249 associated_with POMT1,neuronal migration disorder
54#61#gene5562449#52#diseaseC0457133 12369018-3#54#61#gene55624 12369018-3#49#52#diseaseC0457133 associated_with POMGnT1,MEB
6#13#gene55624141#144#diseaseC0265221 12369018-9#6#13#gene55624 12369018-9#141#144#diseaseC0265221 associated_with POMGnT1,WWS
71#74#gene5562462#66#diseaseC0410174 12369018-8#71#74#gene55624 12369018-8#62#66#diseaseC0410174 associated_with MEB,FCMD