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PubMed:10076558 JSONTXT

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PMID_GLOBAL

Id Subject Object Predicate Lexical cue mondo_id
T1 117-153 DiseaseOrPhenotypicFeature denotes multiple endocrine neoplasia type 2B 0008082
T2 182-210 DiseaseOrPhenotypicFeature denotes Multiple endocrine neoplasia 0017169
T3 212-215 DiseaseOrPhenotypicFeature denotes MEN 0017169
T4 286-289 DiseaseOrPhenotypicFeature denotes MEN 0017169
T5 292-301 DiseaseOrPhenotypicFeature denotes syndromes 0002254
T6 322-325 DiseaseOrPhenotypicFeature denotes MEN 0017169
T7 442-445 DiseaseOrPhenotypicFeature denotes MEN 0017169
T8 714-717 DiseaseOrPhenotypicFeature denotes MEN 0017169
T9 804-840 DiseaseOrPhenotypicFeature denotes familial medullary thyroid carcinoma 0007958

DisGeNET5_variant_disease

Id Subject Object Predicate Lexical cue
10076558-6#13#18#geners79658334 734-739 geners79658334 denotes V804M
10076558-6#83#119#diseaseC1833921 804-840 diseaseC1833921 denotes familial medullary thyroid carcinoma
13#18#geners7965833483#119#diseaseC1833921 10076558-6#13#18#geners79658334 10076558-6#83#119#diseaseC1833921 associated_with V804M,familial medullary thyroid carcinoma

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
10076558-0#61#79#gene5979 61-79 gene5979 denotes RET proto-oncogene
10076558-0#117#153#diseaseC0025269 117-153 diseaseC0025269 denotes multiple endocrine neoplasia type 2B
61#79#gene5979117#153#diseaseC0025269 10076558-0#61#79#gene5979 10076558-0#117#153#diseaseC0025269 associated_with RET proto-oncogene,multiple endocrine neoplasia type 2B

PubmedHPO

Id Subject Object Predicate Lexical cue
T1 191-210 HP_0100568 denotes endocrine neoplasia
T2 201-210 HP_0002664 denotes neoplasia
T3 267-285 HP_0000006 denotes autosomal dominant
T4 813-840 HP_0002865 denotes medullary thyroid carcinoma
T5 823-840 HP_0002890 denotes thyroid carcinoma