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PubMed:9932968 JSONTXT

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DisGeNET

Id Subject Object Predicate Lexical cue
T0 250-253 gene:4137 denotes tau
T1 174-177 disease:C0038868 denotes PSP
T2 250-253 gene:4137 denotes tau
T3 142-172 disease:C0038868 denotes progressive supranuclear palsy
T4 324-327 gene:4137 denotes tau
T5 343-346 disease:C0038868 denotes PSP
R1 T0 T1 associated_with tau,PSP
R2 T2 T3 associated_with tau,progressive supranuclear palsy
R3 T4 T5 associated_with tau,PSP

DisGeNET5_variant_disease

Id Subject Object Predicate Lexical cue
9932968-0#14#19#geners63750424 14-19 geners63750424 denotes R406W
9932968-0#36#66#diseaseC0038868 36-66 diseaseC0038868 denotes progressive supranuclear palsy
9932968-0#71#96#diseaseC0393570 71-96 diseaseC0393570 denotes corticobasal degeneration
9932968-4#28#33#geners63750424 541-546 geners63750424 denotes R406W
9932968-4#137#146#diseaseC0949664 650-659 diseaseC0949664 denotes tauopathy
14#19#geners6375042436#66#diseaseC0038868 9932968-0#14#19#geners63750424 9932968-0#36#66#diseaseC0038868 associated_with R406W,progressive supranuclear palsy
14#19#geners6375042471#96#diseaseC0393570 9932968-0#14#19#geners63750424 9932968-0#71#96#diseaseC0393570 associated_with R406W,corticobasal degeneration
28#33#geners63750424137#146#diseaseC0949664 9932968-4#28#33#geners63750424 9932968-4#137#146#diseaseC0949664 associated_with R406W,tauopathy

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
9932968-2#64#67#gene4137 324-327 gene4137 denotes tau
9932968-2#83#86#diseaseC0038868 343-346 diseaseC0038868 denotes PSP
64#67#gene413783#86#diseaseC0038868 9932968-2#64#67#gene4137 9932968-2#83#86#diseaseC0038868 associated_with tau,PSP