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PubMed:7191069 JSONTXT

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sentences

Id Subject Object Predicate Lexical cue
TextSentencer_T1 0-49 Sentence denotes Heterozygous C2-deficiency and myasthenia gravis.
TextSentencer_T2 50-139 Sentence denotes Complement deficiency states in myasthenia gravis (MG) have not been reported previously.
TextSentencer_T3 140-282 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.
T1 0-49 Sentence denotes Heterozygous C2-deficiency and myasthenia gravis.
T2 50-139 Sentence denotes Complement deficiency states in myasthenia gravis (MG) have not been reported previously.
T3 140-282 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.

PubCasesHPO

Id Subject Object Predicate Lexical cue
AB1 50-71 HP:0004431 denotes Complement deficiency

PubCasesORDO

Id Subject Object Predicate Lexical cue
TI1 31-48 ORDO:589 denotes myasthenia gravis
AB1 82-99 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
T3 50-71 Modifier:D007153 denotes Complement deficiency
T4 82-99 SpecificDisease:D009157 denotes myasthenia gravis
T5 101-103 SpecificDisease:D009157 denotes MG
T6 185-187 SpecificDisease:D009157 denotes MG
T7 205-218 SpecificDisease:OMIM:217000 denotes C2 deficiency

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
T4364 50-71 Modifier denotes Complement deficiency D007153
T4365 82-99 SpecificDisease denotes myasthenia gravis D009157
T4366 101-103 SpecificDisease denotes MG D009157
T4367 185-187 SpecificDisease denotes MG D009157
T4368 205-218 SpecificDisease denotes C2 deficiency OMIM:217000

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
T4364 50-71 Modifier denotes Complement deficiency D007153
T4365 82-99 SpecificDisease denotes myasthenia gravis D009157
T4366 101-103 SpecificDisease denotes MG D009157
T4367 185-187 SpecificDisease denotes MG D009157
T4368 205-218 SpecificDisease denotes C2 deficiency OMIM:217000

NCBI-Disease-Corpus-2stage-All

Id Subject Object Predicate Lexical cue
T1 31-48 SpecificDisease denotes myasthenia gravis
T2 82-99 SpecificDisease denotes myasthenia gravis
T3 101-103 SpecificDisease denotes MG
T4 185-187 SpecificDisease denotes MG

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
T3 82-99 SpecificDisease denotes myasthenia gravis
T4 101-103 SpecificDisease denotes MG
T5 185-187 SpecificDisease denotes MG
T6 205-218 SpecificDisease denotes C2 deficiency

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
T3 82-99 Modifier denotes myasthenia gravis
T4 185-187 SpecificDisease denotes MG
T5 192-218 SpecificDisease denotes heterozygous C2 deficiency

NCBI-Disease-Corpus-Simple-All

Id Subject Object Predicate Lexical cue
T1 0-48 CompositeMention denotes Heterozygous C2-deficiency and myasthenia gravis
T2 50-78 DiseaseClass denotes Complement deficiency states
T3 82-104 SpecificDisease denotes myasthenia gravis (MG)
T4 185-187 SpecificDisease denotes MG
T5 192-218 CompositeMention denotes heterozygous C2 deficiency