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PubMed:22028770 JSONTXT

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DisGeNET

Id Subject Object Predicate Lexical cue
T0 1633-1637 gene:348 denotes APOE
T1 1675-1690 disease:C0011860 denotes type 2 diabetes
T2 1729-1733 gene:348 denotes APOE
T3 1847-1862 disease:C0011860 denotes type 2 diabetes
T4 2166-2170 gene:348 denotes APOE
T5 2189-2204 disease:C0011860 denotes type 2 diabetes
R1 T0 T1 associated_with APOE,type 2 diabetes
R2 T2 T3 associated_with APOE,type 2 diabetes
R3 T4 T5 associated_with APOE,type 2 diabetes

Allie

Id Subject Object Predicate Lexical cue
SS1_22028770_2_0 158-179 expanded denotes apolipoprotein E gene
SS2_22028770_2_0 181-185 abbr denotes APOE
SS1_22028770_3_0 327-357 expanded denotes single nucleotide polymorphism
SS2_22028770_3_0 359-362 abbr denotes SNP
SS1_22028770_9_0 1197-1234 expanded denotes Electrophoretic-mobility-shift assays
SS2_22028770_9_0 1236-1240 abbr denotes EMSA
SS1_22028770_9_1 1246-1276 expanded denotes chromatin immuno-precipitation
SS2_22028770_9_1 1278-1282 abbr denotes ChIP
AE1_22028770_2_0 SS1_22028770_2_0 SS2_22028770_2_0 abbreviatedTo apolipoprotein E gene,APOE
AE1_22028770_3_0 SS1_22028770_3_0 SS2_22028770_3_0 abbreviatedTo single nucleotide polymorphism,SNP
AE1_22028770_9_0 SS1_22028770_9_0 SS2_22028770_9_0 abbreviatedTo Electrophoretic-mobility-shift assays,EMSA
AE1_22028770_9_1 SS1_22028770_9_1 SS2_22028770_9_1 abbreviatedTo chromatin immuno-precipitation,ChIP

PubmedHPO

Id Subject Object Predicate Lexical cue
T1 229-248 HP_0002511 denotes Alzheimer's disease
T2 427-446 HP_0002511 denotes Alzheimer's disease

DisGeNET5_variant_disease

Id Subject Object Predicate Lexical cue
22028770-11#74#82#geners405509 1766-1774 geners405509 denotes rs405509
22028770-11#98#106#geners440446 1790-1798 geners440446 denotes rs440446
22028770-11#155#170#diseaseC0011860 1847-1862 diseaseC0011860 denotes type 2 diabetes
74#82#geners405509155#170#diseaseC0011860 22028770-11#74#82#geners405509 22028770-11#155#170#diseaseC0011860 associated_with rs405509,type 2 diabetes
98#106#geners440446155#170#diseaseC0011860 22028770-11#98#106#geners440446 22028770-11#155#170#diseaseC0011860 associated_with rs440446,type 2 diabetes

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
22028770-1#4#20#gene348 158-174 gene348 denotes apolipoprotein E
22028770-1#117#139#diseaseC0010054 271-293 diseaseC0010054 denotes coronary heart disease
22028770-1#117#139#diseaseC0010068 271-293 diseaseC0010068 denotes coronary heart disease
22028770-1#117#139#diseaseC1956346 271-293 diseaseC1956346 denotes coronary heart disease
22028770-14#86#90#gene348 2166-2170 gene348 denotes APOE
22028770-14#109#124#diseaseC0011860 2189-2204 diseaseC0011860 denotes type 2 diabetes
22028770-2#76#80#gene348 371-375 gene348 denotes APOE
22028770-2#132#151#diseaseC0002395 427-446 diseaseC0002395 denotes Alzheimer's disease
4#20#gene348117#139#diseaseC0010054 22028770-1#4#20#gene348 22028770-1#117#139#diseaseC0010054 associated_with apolipoprotein E,coronary heart disease
4#20#gene348117#139#diseaseC0010068 22028770-1#4#20#gene348 22028770-1#117#139#diseaseC0010068 associated_with apolipoprotein E,coronary heart disease
4#20#gene348117#139#diseaseC1956346 22028770-1#4#20#gene348 22028770-1#117#139#diseaseC1956346 associated_with apolipoprotein E,coronary heart disease
86#90#gene348109#124#diseaseC0011860 22028770-14#86#90#gene348 22028770-14#109#124#diseaseC0011860 associated_with APOE,type 2 diabetes
76#80#gene348132#151#diseaseC0002395 22028770-2#76#80#gene348 22028770-2#132#151#diseaseC0002395 associated_with APOE,Alzheimer's disease

tmVarCorpus

Id Subject Object Predicate Lexical cue
T1 49-57 DNAMutation:c|SUB|A|-491|T denotes -491 A/T
T2 745-752 DNAMutation:c|SUB|A|-491|T denotes -491A/T
T3 754-762 SNP:rs449647 denotes rs449647
T4 857-868 DNAMutation:c|SUB|A|-491|T denotes -491 A to T
T5 1553-1560 DNAMutation:c|SUB|A|-491|T denotes -491A/T
T6 1748-1755 DNAMutation:c|SUB|A|-491|T denotes -491A/T
T7 1757-1764 DNAMutation:c|SUB|G|-219|T denotes -219G/T
T8 1766-1774 SNP:rs405509 denotes rs405509
T9 1781-1788 DNAMutation:c|SUB|G|+113|C denotes +113G/C
T10 1790-1798 SNP:rs440446 denotes rs440446
T11 2011-2018 DNAMutation:c|SUB|A|-491|T denotes -491A/T