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PubMed:10581038 / 0-215 JSONTXT

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c_corpus

Id Subject Object Predicate Lexical cue
T2 0-3 CHEBI:16768 denotes Msh
T6 0-3 D009074 denotes Msh
T7 0-3 D009074 denotes Msh
T8 0-4 PR:000010666 denotes Msh2
T9 0-4 PR:P25847 denotes Msh2
T10 0-4 PR:P43246 denotes Msh2
T11 0-4 P22711 denotes Msh2
T12 0-4 PR:P22711 denotes Msh2
T13 0-4 PR:P54275 denotes Msh2
T14 0-4 PR:O74773 denotes Msh2
T15 0-4 PR:P43247 denotes Msh2
T16 0-4 PR:Q553L4 denotes Msh2
T17 0-4 PR:O24617 denotes Msh2
T18 5-15 SO:1000029 denotes deficiency
T19 60-63 CVCL_D569 denotes CAG
T20 64-70 SO:0001068 denotes repeat
T23 74-92 D006816 denotes Huntington disease
T24 74-92 D006816 denotes Huntington disease
T27 93-103 SO:0000781 denotes transgenic
T28 93-108 10090 denotes transgenic mice
T29 93-108 D008822 denotes transgenic mice
T30 104-108 PR:000005054 denotes mice
T32 104-108 O89094 denotes mice
T34 121-128 D004194 denotes disease
T35 121-128 D004194 denotes disease
T36 138-156 C566739 denotes autosomal dominant
T39 170-196 D019636 denotes neurodegenerative disorder
T40 170-196 D019636 denotes neurodegenerative disorder

PubmedHPO

Id Subject Object Predicate Lexical cue
T1 138-156 HP_0000006 denotes autosomal dominant

UseCases_ArguminSci_Discourse

Id Subject Object Predicate Lexical cue
T1 0-109 DRI_Outcome denotes Msh2 deficiency prevents in vivo somatic instability of the CAG repeat in Huntington disease transgenic mice.

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
10581038-0#0#4#gene4436 0-4 gene4436 denotes Msh2
10581038-0#74#92#diseaseC0020179 74-92 diseaseC0020179 denotes Huntington disease
0#4#gene443674#92#diseaseC0020179 10581038-0#0#4#gene4436 10581038-0#74#92#diseaseC0020179 associated_with Msh2,Huntington disease