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PubMed:7191069 / 0-48 JSONTXT

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PubCasesORDO

Id Subject Object Predicate Lexical cue
TI1 31-48 ORDO:589 denotes myasthenia gravis

NCBIDiseaseCorpus

Id Subject Object Predicate Lexical cue
T1 13-26 SpecificDisease:OMIM:217000 denotes C2-deficiency
T2 31-48 SpecificDisease:D009157 denotes myasthenia gravis

NCBI-Disease-Train

Id Subject Object Predicate Lexical cue database_id
T4362 13-26 SpecificDisease denotes C2-deficiency OMIM:217000
T4363 31-48 SpecificDisease denotes myasthenia gravis D009157

NCBI-Disease-Corpus-All

Id Subject Object Predicate Lexical cue database_id
T4362 13-26 SpecificDisease denotes C2-deficiency OMIM:217000
T4363 31-48 SpecificDisease denotes myasthenia gravis D009157

NCBI-Disease-Corpus-2stage-All

Id Subject Object Predicate Lexical cue
T1 31-48 SpecificDisease denotes myasthenia gravis

NCBI-Disease-Corpus-rezarta-All

Id Subject Object Predicate Lexical cue
T1 13-26 SpecificDisease denotes C2-deficiency
T2 31-48 SpecificDisease denotes myasthenia gravis

NCBI-Disease-Corpus-4oGuideline-All

Id Subject Object Predicate Lexical cue
T1 13-26 SpecificDisease denotes C2-deficiency
T2 31-48 SpecificDisease denotes myasthenia gravis

NCBI-Disease-Corpus-Simple-All

Id Subject Object Predicate Lexical cue
T1 0-48 CompositeMention denotes Heterozygous C2-deficiency and myasthenia gravis