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PubMed:24859272 JSONTXT

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Allie

Id Subject Object Predicate Lexical cue
SS1_24859272_2_0 131-162 expanded denotes single nucleotide polymorphisms
SS2_24859272_2_0 164-168 abbr denotes SNPs
SS1_24859272_2_1 220-236 expanded denotes Behcet's disease
SS2_24859272_2_1 238-240 abbr denotes BD
SS1_24859272_2_2 246-266 expanded denotes Vogt-Koyanagi-Harada
SS2_24859272_2_2 268-271 abbr denotes VKH
SS1_24859272_11_0 1091-1108 expanded denotes corrected p value
SS2_24859272_11_0 1110-1112 abbr denotes pc
AE1_24859272_2_0 SS1_24859272_2_0 SS2_24859272_2_0 abbreviatedTo single nucleotide polymorphisms,SNPs
AE1_24859272_2_1 SS1_24859272_2_1 SS2_24859272_2_1 abbreviatedTo Behcet's disease,BD
AE1_24859272_2_2 SS1_24859272_2_2 SS2_24859272_2_2 abbreviatedTo Vogt-Koyanagi-Harada,VKH
AE1_24859272_11_0 SS1_24859272_11_0 SS2_24859272_11_0 abbreviatedTo corrected p value,pc

DisGeNET5_variant_disease

Id Subject Object Predicate Lexical cue
24859272-10#87#96#geners3212227 1491-1500 geners3212227 denotes rs3212227
24859272-10#252#261#geners3212227 1656-1665 geners3212227 denotes rs3212227
24859272-10#109#111#diseaseC0004943 1513-1515 diseaseC0004943 denotes BD
87#96#geners3212227109#111#diseaseC0004943 24859272-10#87#96#geners3212227 24859272-10#109#111#diseaseC0004943 associated_with rs3212227,BD
252#261#geners3212227109#111#diseaseC0004943 24859272-10#252#261#geners3212227 24859272-10#109#111#diseaseC0004943 associated_with rs3212227,BD

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
24859272-0#40#48#gene3595 40-48 gene3595 denotes IL-12Rβ2
24859272-0#52#68#diseaseC0004943 52-68 diseaseC0004943 denotes Behcet's disease
24859272-0#73#85#diseaseC0042170 73-85 diseaseC0042170 denotes VKH syndrome
24859272-1#98#106#gene3594 194-202 gene3594 denotes IL-12Rβ1
24859272-1#124#140#diseaseC0004943 220-236 diseaseC0004943 denotes Behcet's disease
24859272-1#172#185#diseaseC0042170 268-281 diseaseC0042170 denotes VKH) syndrome
24859272-11#28#34#gene3593 1804-1810 gene3593 denotes IL-12B
24859272-11#82#84#diseaseC0004943 1858-1860 diseaseC0004943 denotes BD
24859272-11#96#108#diseaseC0042170 1872-1884 diseaseC0042170 denotes VKH syndrome
40#48#gene359552#68#diseaseC0004943 24859272-0#40#48#gene3595 24859272-0#52#68#diseaseC0004943 associated_with IL-12Rβ2,Behcet's disease
40#48#gene359573#85#diseaseC0042170 24859272-0#40#48#gene3595 24859272-0#73#85#diseaseC0042170 associated_with IL-12Rβ2,VKH syndrome
98#106#gene3594124#140#diseaseC0004943 24859272-1#98#106#gene3594 24859272-1#124#140#diseaseC0004943 associated_with IL-12Rβ1,Behcet's disease
98#106#gene3594172#185#diseaseC0042170 24859272-1#98#106#gene3594 24859272-1#172#185#diseaseC0042170 associated_with IL-12Rβ1,VKH) syndrome
28#34#gene359382#84#diseaseC0004943 24859272-11#28#34#gene3593 24859272-11#82#84#diseaseC0004943 associated_with IL-12B,BD
28#34#gene359396#108#diseaseC0042170 24859272-11#28#34#gene3593 24859272-11#96#108#diseaseC0042170 associated_with IL-12B,VKH syndrome