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PubMed:12191970 JSONTXT

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DisGeNET5_variant_disease

Id Subject Object Predicate Lexical cue
12191970-4#90#95#geners104893708 847-852 geners104893708 denotes L125P
12191970-4#38#41#diseaseC1332347 795-798 diseaseC1332347 denotes ADH
12191970-7#31#36#geners104893708 1488-1493 geners104893708 denotes L125P
12191970-7#226#254#diseaseC0271728 1683-1711 diseaseC0271728 denotes secondary hyperaldosteronism
90#95#geners10489370838#41#diseaseC1332347 12191970-4#90#95#geners104893708 12191970-4#38#41#diseaseC1332347 associated_with L125P,ADH
31#36#geners104893708226#254#diseaseC0271728 12191970-7#31#36#geners104893708 12191970-7#226#254#diseaseC0271728 associated_with L125P,secondary hyperaldosteronism

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
12191970-0#33#57#gene846 33-57 gene846 denotes calcium-sensing receptor
12191970-0#77#108#diseaseC4048195 77-108 diseaseC4048195 denotes autosomal dominant hypocalcemia
33#57#gene84677#108#diseaseC4048195 12191970-0#33#57#gene846 12191970-0#77#108#diseaseC4048195 associated_with calcium-sensing receptor,autosomal dominant hypocalcemia

PubCasesHPO

Id Subject Object Predicate Lexical cue
TI1 96-108 HP:0002901 denotes hypocalcemia
AB1 601-613 HP:0002901 denotes hypocalcemia
AB2 1017-1045 HP:0011741 denotes secondary hyperaldosteronism
AB3 1050-1061 HP:0002900 denotes hypokalemia
AB4 1683-1711 HP:0011741 denotes secondary hyperaldosteronism
AB5 1716-1727 HP:0002900 denotes hypokalemia

DisGeNET

Id Subject Object Predicate Lexical cue
T0 33-57 gene:846 denotes calcium-sensing receptor
T1 77-108 disease:C0342345 denotes autosomal dominant hypocalcemia
R1 T0 T1 associated_with calcium-sensing receptor,autosomal dominant hypocalcemia