PubMed:7643352 JSONTXT 11 Projects

Annnotations TAB TSV DIC JSON TextAE Lectin_function IAV-Glycan

Id Subject Object Predicate Lexical cue
7643352-9#24#29#gene1678 1095-1100 gene1678 denotes DFN-1
7643352-9#160#178#diseaseC0155320 1231-1249 diseaseC0155320 denotes cortical blindness
7643352-9#205#222#diseaseC0917816 1276-1293 diseaseC0917816 denotes mental deficiency
7643352-12#126#129#gene5354 1694-1697 gene5354 denotes PMD
7643352-12#131#159#diseaseC0205711 1699-1727 diseaseC0205711 denotes Pelizaeus-Merzbacher disease
7643352-12#187#216#diseaseC0037773 1755-1784 diseaseC0037773 denotes hereditary spastic paraplegia
126#129#gene5354131#159#diseaseC0205711 7643352-12#126#129#gene5354 7643352-12#131#159#diseaseC0205711 associated_with PMD,Pelizaeus-Merzbacher disease
126#129#gene5354187#216#diseaseC0037773 7643352-12#126#129#gene5354 7643352-12#187#216#diseaseC0037773 associated_with PMD,hereditary spastic paraplegia
24#29#gene1678160#178#diseaseC0155320 7643352-9#24#29#gene1678 7643352-9#160#178#diseaseC0155320 associated_with DFN-1,cortical blindness
24#29#gene1678205#222#diseaseC0917816 7643352-9#24#29#gene1678 7643352-9#205#222#diseaseC0917816 associated_with DFN-1,mental deficiency