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PubMed:7191069 / 140-282 JSONTXT

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sentences

Id Subject Object Predicate Lexical cue
TextSentencer_T3 0-142 Sentence denotes We describe a 19-year-old woman with typical MG and heterozygous C2 deficiency, along with HLA typing of the patient and her immediate family.
T3 0-142 Sentence denotes We describe a 19-year-old woman with typical MG and heterozygous C2 deficiency, along with HLA typing of the patient and her immediate family.

NCBIDiseaseCorpus

Id Subject Object Predicate Lexical cue
T6 45-47 SpecificDisease:D009157 denotes MG
T7 65-78 SpecificDisease:OMIM:217000 denotes C2 deficiency

NCBI-Disease-Train

Id Subject Object Predicate Lexical cue database_id
T4367 45-47 SpecificDisease denotes MG D009157
T4368 65-78 SpecificDisease denotes C2 deficiency OMIM:217000

NCBI-Disease-Corpus-All

Id Subject Object Predicate Lexical cue database_id
T4367 45-47 SpecificDisease denotes MG D009157
T4368 65-78 SpecificDisease denotes C2 deficiency OMIM:217000

NCBI-Disease-Corpus-2stage-All

Id Subject Object Predicate Lexical cue
T4 45-47 SpecificDisease denotes MG

NCBI-Disease-Corpus-rezarta-All

Id Subject Object Predicate Lexical cue
T5 45-47 SpecificDisease denotes MG
T6 65-78 SpecificDisease denotes C2 deficiency

NCBI-Disease-Corpus-4oGuideline-All

Id Subject Object Predicate Lexical cue
T4 45-47 SpecificDisease denotes MG
T5 52-78 SpecificDisease denotes heterozygous C2 deficiency

NCBI-Disease-Corpus-Simple-All

Id Subject Object Predicate Lexical cue
T4 45-47 SpecificDisease denotes MG
T5 52-78 CompositeMention denotes heterozygous C2 deficiency