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PubMed:19882638 JSONTXT

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Allie

Id Subject Object Predicate Lexical cue
SS1_19882638_4_0 655-672 expanded denotes electromyographic
SS2_19882638_4_0 674-677 abbr denotes EMG
SS1_19882638_5_0 837-870 expanded denotes compound muscle action potentials
SS2_19882638_5_0 872-877 abbr denotes CMAPs
AE1_19882638_4_0 SS1_19882638_4_0 SS2_19882638_4_0 abbreviatedTo electromyographic,EMG
AE1_19882638_5_0 SS1_19882638_5_0 SS2_19882638_5_0 abbreviatedTo compound muscle action potentials,CMAPs

DisGeNET

Id Subject Object Predicate Lexical cue
T0 556-561 gene:1180 denotes CLCN1
T1 480-498 disease:C0027127 denotes myotonia congenita
T2 556-561 gene:1180 denotes CLCN1
T3 480-498 disease:C2936781 denotes myotonia congenita
R1 T0 T1 associated_with CLCN1,myotonia congenita
R2 T2 T3 associated_with CLCN1,myotonia congenita

DisGeNET5_variant_disease

Id Subject Object Predicate Lexical cue
19882638-3#152#157#geners80356697 562-567 geners80356697 denotes I556N
19882638-3#70#88#diseaseC0027127 480-498 diseaseC0027127 denotes myotonia congenita
19882638-3#70#88#diseaseC2936781 480-498 diseaseC2936781 denotes myotonia congenita
152#157#geners8035669770#88#diseaseC0027127 19882638-3#152#157#geners80356697 19882638-3#70#88#diseaseC0027127 associated_with I556N,myotonia congenita
152#157#geners8035669770#88#diseaseC2936781 19882638-3#152#157#geners80356697 19882638-3#70#88#diseaseC2936781 associated_with I556N,myotonia congenita