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PubMed:16979952 JSONTXT

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PubTator4TogoVar

Id Subject Object Predicate Lexical cue proteinmutation
16979952_0 58-63 ProteinMutation denotes C282Y rs1800562
16979952_1 68-72 ProteinMutation denotes H63D rs1799945
16979952_2 224-229 ProteinMutation denotes C282Y rs1800562
16979952_3 306-311 ProteinMutation denotes C282Y rs1800562
16979952_4 312-316 ProteinMutation denotes H63D rs1799945
16979952_5 389-394 ProteinMutation denotes C282Y rs1800562
16979952_6 395-399 ProteinMutation denotes H63D rs1799945
16979952_7 426-431 ProteinMutation denotes C282Y rs1800562
16979952_8 481-486 ProteinMutation denotes C282Y rs1800562
16979952_9 487-491 ProteinMutation denotes H63D rs1799945
16979952_10 506-511 ProteinMutation denotes C282Y rs1800562
16979952_11 512-516 ProteinMutation denotes H63D rs1799945
16979952_12 571-576 ProteinMutation denotes C282Y rs1800562
16979952_13 732-737 ProteinMutation denotes C282Y rs1800562
16979952_14 738-742 ProteinMutation denotes H63D rs1799945
16979952_15 816-821 ProteinMutation denotes C282Y rs1800562
16979952_16 872-877 ProteinMutation denotes C282Y rs1800562
16979952_17 878-882 ProteinMutation denotes H63D rs1799945
16979952_18 900-905 ProteinMutation denotes C282Y rs1800562
16979952_19 906-910 ProteinMutation denotes H63D rs1799945
16979952_20 975-980 ProteinMutation denotes C282Y rs1800562
16979952_21 981-985 ProteinMutation denotes H63D rs1799945
16979952_22 1149-1154 ProteinMutation denotes C282Y rs1800562
16979952_23 1155-1159 ProteinMutation denotes H63D rs1799945
16979952_24 1460-1465 ProteinMutation denotes C282Y rs1800562
16979952_25 1552-1557 ProteinMutation denotes C282Y rs1800562
16979952_26 1558-1562 ProteinMutation denotes H63D rs1799945
16979952_27 1597-1602 ProteinMutation denotes C282Y rs1800562
16979952_28 1629-1634 ProteinMutation denotes C282Y rs1800562
16979952_29 1635-1639 ProteinMutation denotes H63D rs1799945
16979952_30 2046-2051 ProteinMutation denotes C282Y rs1800562

DisGeNET5_variant_disease

Id Subject Object Predicate Lexical cue
16979952-0#58#63#geners1800562 58-63 geners1800562 denotes C282Y
16979952-0#68#72#geners1799945 68-72 geners1799945 denotes H63D
16979952-0#90#105#diseaseC0018995 90-105 diseaseC0018995 denotes hemochromatosis
16979952-0#90#105#diseaseC3469186 90-105 diseaseC3469186 denotes hemochromatosis
16979952-0#90#105#diseaseC0018995 90-105 diseaseC0018995 denotes hemochromatosis
16979952-0#90#105#diseaseC3469186 90-105 diseaseC3469186 denotes hemochromatosis
16979952-13#6#10#geners1799945 1635-1639 geners1799945 denotes H63D
16979952-13#174#183#diseaseC2711227 1803-1812 diseaseC2711227 denotes steatosis
16979952-9#16#20#geners1799945 1155-1159 geners1799945 denotes H63D
16979952-9#137#153#diseaseC0239946 1276-1292 diseaseC0239946 denotes hepatic fibrosis
58#63#geners180056290#105#diseaseC0018995 16979952-0#58#63#geners1800562 16979952-0#90#105#diseaseC0018995 associated_with C282Y,hemochromatosis
58#63#geners180056290#105#diseaseC3469186 16979952-0#58#63#geners1800562 16979952-0#90#105#diseaseC3469186 associated_with C282Y,hemochromatosis
58#63#geners180056290#105#diseaseC0018995 16979952-0#58#63#geners1800562 16979952-0#90#105#diseaseC0018995 associated_with C282Y,hemochromatosis
58#63#geners180056290#105#diseaseC3469186 16979952-0#58#63#geners1800562 16979952-0#90#105#diseaseC3469186 associated_with C282Y,hemochromatosis
68#72#geners179994590#105#diseaseC0018995 16979952-0#68#72#geners1799945 16979952-0#90#105#diseaseC0018995 associated_with H63D,hemochromatosis
68#72#geners179994590#105#diseaseC3469186 16979952-0#68#72#geners1799945 16979952-0#90#105#diseaseC3469186 associated_with H63D,hemochromatosis
68#72#geners179994590#105#diseaseC0018995 16979952-0#68#72#geners1799945 16979952-0#90#105#diseaseC0018995 associated_with H63D,hemochromatosis
68#72#geners179994590#105#diseaseC3469186 16979952-0#68#72#geners1799945 16979952-0#90#105#diseaseC3469186 associated_with H63D,hemochromatosis
6#10#geners1799945174#183#diseaseC2711227 16979952-13#6#10#geners1799945 16979952-13#174#183#diseaseC2711227 associated_with H63D,steatosis
16#20#geners1799945137#153#diseaseC0239946 16979952-9#16#20#geners1799945 16979952-9#137#153#diseaseC0239946 associated_with H63D,hepatic fibrosis