PubMed:10023663 JSONTXT 5 Projects

Annnotations TAB TSV DIC JSON TextAE Lectin_function IAV-Glycan

Id Subject Object Predicate Lexical cue
10023663-0#20#35#diseaseC0266292 20-35 diseaseC0266292 denotes renal anomalies
10023663-0#61#64#gene5979 61-64 gene5979 denotes RET
10023663-0#65#70#diseaseC0025269 65-70 diseaseC0025269 denotes MEN2B
10023663-3#23#26#gene5979 424-427 gene5979 denotes RET
10023663-3#62#67#gene5979 463-468 gene5979 denotes MEN2A
10023663-3#121#134#diseaseC0019569 522-535 diseaseC0019569 denotes aganglionosis
10023663-3#121#134#diseaseC0019569 522-535 diseaseC0019569 denotes aganglionosis
10023663-3#136#156#diseaseC0019569 537-557 diseaseC0019569 denotes Hirschsprung disease
10023663-4#39#64#gene1621 599-624 gene1621 denotes dopamine beta-hydroxylase
10023663-4#102#107#diseaseC0025269 662-667 diseaseC0025269 denotes MEN2B
10023663-5#7#10#gene5979 759-762 gene5979 denotes RET
10023663-5#104#119#diseaseC0017075 856-871 diseaseC0017075 denotes ganglioneuromas
10023663-8#25#28#gene27352 1172-1175 gene27352 denotes MAP
10023663-8#66#71#diseaseC0025269 1213-1218 diseaseC0025269 denotes MEN2B
10023663-9#50#53#gene5979 1397-1400 gene5979 denotes RET
10023663-9#102#115#diseaseC0000768 1449-1462 diseaseC0000768 denotes malformations
23#26#gene5979121#134#diseaseC0019569 10023663-3#23#26#gene5979 10023663-3#121#134#diseaseC0019569 associated_with RET,aganglionosis
23#26#gene5979121#134#diseaseC0019569 10023663-3#23#26#gene5979 10023663-3#121#134#diseaseC0019569 associated_with RET,aganglionosis
23#26#gene5979136#156#diseaseC0019569 10023663-3#23#26#gene5979 10023663-3#136#156#diseaseC0019569 associated_with RET,Hirschsprung disease
25#28#gene2735266#71#diseaseC0025269 10023663-8#25#28#gene27352 10023663-8#66#71#diseaseC0025269 associated_with MAP,MEN2B
39#64#gene1621102#107#diseaseC0025269 10023663-4#39#64#gene1621 10023663-4#102#107#diseaseC0025269 associated_with dopamine beta-hydroxylase,MEN2B
50#53#gene5979102#115#diseaseC0000768 10023663-9#50#53#gene5979 10023663-9#102#115#diseaseC0000768 associated_with RET,malformations
61#64#gene597920#35#diseaseC0266292 10023663-0#61#64#gene5979 10023663-0#20#35#diseaseC0266292 associated_with RET,renal anomalies
61#64#gene597965#70#diseaseC0025269 10023663-0#61#64#gene5979 10023663-0#65#70#diseaseC0025269 associated_with RET,MEN2B
62#67#gene5979121#134#diseaseC0019569 10023663-3#62#67#gene5979 10023663-3#121#134#diseaseC0019569 associated_with MEN2A,aganglionosis
62#67#gene5979121#134#diseaseC0019569 10023663-3#62#67#gene5979 10023663-3#121#134#diseaseC0019569 associated_with MEN2A,aganglionosis
62#67#gene5979136#156#diseaseC0019569 10023663-3#62#67#gene5979 10023663-3#136#156#diseaseC0019569 associated_with MEN2A,Hirschsprung disease
7#10#gene5979104#119#diseaseC0017075 10023663-5#7#10#gene5979 10023663-5#104#119#diseaseC0017075 associated_with RET,ganglioneuromas