> top > docs > PubMed:7191069 > spans > 0-142 > annotations

PubMed:7191069 / 0-142 JSONTXT

Annnotations TAB JSON ListView MergeView

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.
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.

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

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

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

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

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

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

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)