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PubMed:10029606 / 732-1011 JSONTXT

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PubTator4TogoVar

Id Subject Object Predicate Lexical cue proteinmutation
10029606_1 117-122 ProteinMutation denotes C282Y rs1800562

sentences

Id Subject Object Predicate Lexical cue
TextSentencer_T6 0-279 Sentence denotes There was a significantly higher frequency of coinheritance of the hereditary hemochromatosis (HH) HFE mutant allele C282Y in 18 unrelated XLSA hemizygotes than found in the normal population, indicating a role for coinheritance of HFE alleles in the expression of this disorder.
T6 0-279 Sentence denotes There was a significantly higher frequency of coinheritance of the hereditary hemochromatosis (HH) HFE mutant allele C282Y in 18 unrelated XLSA hemizygotes than found in the normal population, indicating a role for coinheritance of HFE alleles in the expression of this disorder.

DisGeNET5_variant_disease

Id Subject Object Predicate Lexical cue
10029606-5#117#122#geners1800562 117-122 geners1800562 denotes C282Y
10029606-5#139#143#diseaseC0221018 139-143 diseaseC0221018 denotes XLSA
117#122#geners1800562139#143#diseaseC0221018 10029606-5#117#122#geners1800562 10029606-5#139#143#diseaseC0221018 associated_with C282Y,XLSA

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
10029606-5#99#102#gene3077 99-102 gene3077 denotes HFE
10029606-5#232#235#gene3077 232-235 gene3077 denotes HFE
10029606-5#67#93#diseaseC0392514 67-93 diseaseC0392514 denotes hereditary hemochromatosis
10029606-5#95#97#diseaseC0392514 95-97 diseaseC0392514 denotes HH
10029606-5#139#143#diseaseC0221018 139-143 diseaseC0221018 denotes XLSA
10029606-5#67#93#diseaseC0392514 67-93 diseaseC0392514 denotes hereditary hemochromatosis
10029606-5#95#97#diseaseC0392514 95-97 diseaseC0392514 denotes HH
10029606-5#139#143#diseaseC0221018 139-143 diseaseC0221018 denotes XLSA
99#102#gene307767#93#diseaseC0392514 10029606-5#99#102#gene3077 10029606-5#67#93#diseaseC0392514 associated_with HFE,hereditary hemochromatosis
99#102#gene307795#97#diseaseC0392514 10029606-5#99#102#gene3077 10029606-5#95#97#diseaseC0392514 associated_with HFE,HH
99#102#gene3077139#143#diseaseC0221018 10029606-5#99#102#gene3077 10029606-5#139#143#diseaseC0221018 associated_with HFE,XLSA
99#102#gene307767#93#diseaseC0392514 10029606-5#99#102#gene3077 10029606-5#67#93#diseaseC0392514 associated_with HFE,hereditary hemochromatosis
99#102#gene307795#97#diseaseC0392514 10029606-5#99#102#gene3077 10029606-5#95#97#diseaseC0392514 associated_with HFE,HH
99#102#gene3077139#143#diseaseC0221018 10029606-5#99#102#gene3077 10029606-5#139#143#diseaseC0221018 associated_with HFE,XLSA
232#235#gene307767#93#diseaseC0392514 10029606-5#232#235#gene3077 10029606-5#67#93#diseaseC0392514 associated_with HFE,hereditary hemochromatosis
232#235#gene307795#97#diseaseC0392514 10029606-5#232#235#gene3077 10029606-5#95#97#diseaseC0392514 associated_with HFE,HH
232#235#gene3077139#143#diseaseC0221018 10029606-5#232#235#gene3077 10029606-5#139#143#diseaseC0221018 associated_with HFE,XLSA
232#235#gene307767#93#diseaseC0392514 10029606-5#232#235#gene3077 10029606-5#67#93#diseaseC0392514 associated_with HFE,hereditary hemochromatosis
232#235#gene307795#97#diseaseC0392514 10029606-5#232#235#gene3077 10029606-5#95#97#diseaseC0392514 associated_with HFE,HH
232#235#gene3077139#143#diseaseC0221018 10029606-5#232#235#gene3077 10029606-5#139#143#diseaseC0221018 associated_with HFE,XLSA

PubCasesORDO

Id Subject Object Predicate Lexical cue
AB4 139-143 ORDO:75563 denotes XLSA