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PubMed:7581380 / 219-265 JSONTXT

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DisGeNET

Id Subject Object Predicate Lexical cue
T1 9-27 disease:C2936781 denotes myotonia congenita
T3 9-27 disease:C0027127 denotes myotonia congenita

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
7581380-2#0#46#diseaseC2936781 0-46 diseaseC2936781 denotes Dominant myotonia congenita (Thomsen's disease

NCBIDiseaseCorpus

Id Subject Object Predicate Lexical cue
T4 0-27 SpecificDisease:D009224 denotes Dominant myotonia congenita
T5 29-46 SpecificDisease:D009224 denotes Thomsen's disease

NCBI-Disease-Train

Id Subject Object Predicate Lexical cue database_id
T1316 0-27 SpecificDisease denotes Dominant myotonia congenita D009224
T1317 29-46 SpecificDisease denotes Thomsen's disease D009224

NCBI-Disease-Corpus-All

Id Subject Object Predicate Lexical cue database_id
T1316 0-27 SpecificDisease denotes Dominant myotonia congenita D009224
T1317 29-46 SpecificDisease denotes Thomsen's disease D009224

NCBI-Disease-Corpus-2stage-All

Id Subject Object Predicate Lexical cue
T3 9-27 SpecificDisease denotes myotonia congenita
T4 29-46 SpecificDisease denotes Thomsen's disease

NCBI-Disease-Corpus-rezarta-All

Id Subject Object Predicate Lexical cue
T3 9-27 SpecificDisease denotes myotonia congenita
T4 29-46 SpecificDisease denotes Thomsen's disease