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PubMed:22658899 JSONTXT

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DisGeNET

Id Subject Object Predicate Lexical cue
T0 46-59 gene:5621 denotes prion protein
T1 15-40 disease:C0022336 denotes Creutzfeldt-Jakob disease
T2 316-329 gene:5621 denotes prion protein
T3 307-310 disease:C0022336 denotes CJD
T4 316-329 gene:5621 denotes prion protein
T5 231-256 disease:C0022336 denotes Creutzfeldt-Jakob disease
T6 316-329 gene:5621 denotes prion protein
T7 360-363 disease:C0022336 denotes CJD
R1 T0 T1 associated_with prion protein,Creutzfeldt-Jakob disease
R2 T2 T3 associated_with prion protein,CJD
R3 T4 T5 associated_with prion protein,Creutzfeldt-Jakob disease
R4 T6 T7 associated_with prion protein,CJD

PubmedHPO

Id Subject Object Predicate Lexical cue
T1 584-593 HP_0001336 denotes myoclonus
T2 664-673 HP_0001336 denotes myoclonus
T3 836-851 HP_0012672 denotes akinetic mutism
T4 845-851 HP_0002300 denotes mutism

Allie

Id Subject Object Predicate Lexical cue
SS1_22658899_1_0 231-256 expanded denotes Creutzfeldt-Jakob disease
SS2_22658899_1_0 258-261 abbr denotes CJD
AE1_22658899_1_0 SS1_22658899_1_0 SS2_22658899_1_0 abbreviatedTo Creutzfeldt-Jakob disease,CJD

DisGeNET5_variant_disease

Id Subject Object Predicate Lexical cue
22658899-7#138#143#geners74315408 1254-1259 geners74315408 denotes V180I
22658899-7#144#147#diseaseC0022336 1260-1263 diseaseC0022336 denotes CJD
138#143#geners74315408144#147#diseaseC0022336 22658899-7#138#143#geners74315408 22658899-7#144#147#diseaseC0022336 associated_with V180I,CJD

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
22658899-0#46#59#gene5621 46-59 gene5621 denotes prion protein
22658899-0#15#40#diseaseC0022336 15-40 diseaseC0022336 denotes Creutzfeldt-Jakob disease
46#59#gene562115#40#diseaseC0022336 22658899-0#46#59#gene5621 22658899-0#15#40#diseaseC0022336 associated_with prion protein,Creutzfeldt-Jakob disease

PubCasesHPO

Id Subject Object Predicate Lexical cue
AB1 584-593 HP:0001336 denotes myoclonus
AB2 664-673 HP:0001336 denotes myoclonus
AB3 836-851 HP:0012672 denotes akinetic mutism