PubMed:11494364 / 1402-1535 JSONTXT

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c_corpus

Id Subject Object Predicate Lexical cue
T123 4-7 CVCL_D569 denotes CAG
T124 8-14 SO:0001068 denotes repeat
T125 43-47 P47819 denotes GFAP
T127 43-47 P14136 denotes GFAP
T128 43-47 PR:P03995 denotes GFAP
T129 43-47 PR:000007939 denotes GFAP
T130 43-47 PR:P47819 denotes GFAP
T131 43-47 Q28115 denotes GFAP
T132 43-47 Q58EE9 denotes GFAP
T133 43-47 PR:P14136 denotes GFAP
T134 43-47 Q5RA72 denotes GFAP
T135 43-47 P03995 denotes GFAP
T136 43-47 P48677 denotes GFAP
T137 43-47 PR:Q58EE9 denotes GFAP
T126 43-47 GO:0045101 denotes GFAP
T138 71-76 10090 denotes mouse
T139 71-76 D051379 denotes mouse

UseCases_ArguminSci_Discourse

Id Subject Object Predicate Lexical cue
T10 0-133 DRI_Outcome denotes The CAG repeat instability and increase in GFAP-positive cells in this mouse model appear to mirror the abnormalities in HD patients.

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
11494364-9#43#47#gene2670 43-47 gene2670 denotes GFAP
11494364-9#121#123#diseaseC0020179 121-123 diseaseC0020179 denotes HD
43#47#gene2670121#123#diseaseC0020179 11494364-9#43#47#gene2670 11494364-9#121#123#diseaseC0020179 associated_with GFAP,HD