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PubMed:15171721 JSONTXT 5 Projects

Annnotations TAB TSV DIC JSON TextAE Lectin_function IAV-Glycan

Id Subject Object Predicate Lexical cue
15171721-4#92#98#geners2076738 843-849 geners2076738 denotes C1264R
15171721-4#103#109#geners2076739 854-860 geners2076739 denotes C1996S
15171721-4#168#193#diseaseC0010308 919-944 diseaseC0010308 denotes congenital hypothyroidism
15171721-4#168#193#diseaseC0010308 919-944 diseaseC0010308 denotes congenital hypothyroidism
15171721-4#201#206#diseaseC0013336 952-957 diseaseC0013336 denotes dwarf
15171721-4#201#206#diseaseC0013336 952-957 diseaseC0013336 denotes dwarf
103#109#geners2076739168#193#diseaseC0010308 15171721-4#103#109#geners2076739 15171721-4#168#193#diseaseC0010308 associated_with C1996S,congenital hypothyroidism
103#109#geners2076739168#193#diseaseC0010308 15171721-4#103#109#geners2076739 15171721-4#168#193#diseaseC0010308 associated_with C1996S,congenital hypothyroidism
103#109#geners2076739201#206#diseaseC0013336 15171721-4#103#109#geners2076739 15171721-4#201#206#diseaseC0013336 associated_with C1996S,dwarf
103#109#geners2076739201#206#diseaseC0013336 15171721-4#103#109#geners2076739 15171721-4#201#206#diseaseC0013336 associated_with C1996S,dwarf
92#98#geners2076738168#193#diseaseC0010308 15171721-4#92#98#geners2076738 15171721-4#168#193#diseaseC0010308 associated_with C1264R,congenital hypothyroidism
92#98#geners2076738168#193#diseaseC0010308 15171721-4#92#98#geners2076738 15171721-4#168#193#diseaseC0010308 associated_with C1264R,congenital hypothyroidism
92#98#geners2076738201#206#diseaseC0013336 15171721-4#92#98#geners2076738 15171721-4#201#206#diseaseC0013336 associated_with C1264R,dwarf
92#98#geners2076738201#206#diseaseC0013336 15171721-4#92#98#geners2076738 15171721-4#201#206#diseaseC0013336 associated_with C1264R,dwarf