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PubMed:8466512 JSONTXT

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sentences

Id Subject Object Predicate Lexical cue
TextSentencer_T1 0-88 Sentence denotes A novel disease with deficiency of mitochondrial very-long-chain acyl-CoA dehydrogenase.
TextSentencer_T2 89-357 Sentence denotes Palmitoyl-CoA dehydrogenase activity in skin fibroblasts from seven patients with unidentified defects of fatty acid oxidation was measured in the presence and absence of antibodies against medium-chain, long-chain, and very-long-chain acyl-CoA dehydrogenases (VLCAD).
TextSentencer_T3 358-603 Sentence denotes Two of the patients, 4-5 month old boys, were found to have a novel disease, VLCAD deficiency, as judged from the results of very low palmitoyl-CoA dehydrogenase activity and the lack of immunoreactivity toward antibody raised to purified VLCAD.
T1 0-88 Sentence denotes A novel disease with deficiency of mitochondrial very-long-chain acyl-CoA dehydrogenase.
T2 89-357 Sentence denotes Palmitoyl-CoA dehydrogenase activity in skin fibroblasts from seven patients with unidentified defects of fatty acid oxidation was measured in the presence and absence of antibodies against medium-chain, long-chain, and very-long-chain acyl-CoA dehydrogenases (VLCAD).
T3 358-603 Sentence denotes Two of the patients, 4-5 month old boys, were found to have a novel disease, VLCAD deficiency, as judged from the results of very low palmitoyl-CoA dehydrogenase activity and the lack of immunoreactivity toward antibody raised to purified VLCAD.

PubCasesORDO

Id Subject Object Predicate Lexical cue
AB1 435-451 ORDO:26793 denotes VLCAD deficiency

NCBIDiseaseCorpus

Id Subject Object Predicate Lexical cue
T1 21-87 SpecificDisease:C536353 denotes deficiency of mitochondrial very-long-chain acyl-CoA dehydrogenase
T2 435-451 SpecificDisease:C536353 denotes VLCAD deficiency

NCBI-Disease-Train

Id Subject Object Predicate Lexical cue database_id
T2241 21-87 SpecificDisease denotes deficiency of mitochondrial very-long-chain acyl-CoA dehydrogenase C536353
T2242 435-451 SpecificDisease denotes VLCAD deficiency C536353

NCBI-Disease-Corpus-All

Id Subject Object Predicate Lexical cue database_id
T2241 21-87 SpecificDisease denotes deficiency of mitochondrial very-long-chain acyl-CoA dehydrogenase C536353
T2242 435-451 SpecificDisease denotes VLCAD deficiency C536353

NCBI-Disease-Corpus-2stage-All

Id Subject Object Predicate Lexical cue
T1 8-15 DiseaseClass denotes disease
T2 350-355 Modifier denotes VLCAD
T3 426-433 DiseaseClass denotes disease
T4 435-451 SpecificDisease denotes VLCAD deficiency
T5 597-602 SpecificDisease denotes VLCAD

NCBI-Disease-Corpus-rezarta-All

Id Subject Object Predicate Lexical cue
T1 49-87 DiseaseClass denotes very-long-chain acyl-CoA dehydrogenase
T2 279-291 Modifier denotes medium-chain
T3 293-303 Modifier denotes long-chain
T4 309-348 Modifier denotes very-long-chain acyl-CoA dehydrogenases
T5 350-355 Modifier denotes VLCAD
T6 435-451 SpecificDisease denotes VLCAD deficiency
T7 597-602 Modifier denotes VLCAD

NCBI-Disease-Corpus-4oGuideline-All

Id Subject Object Predicate Lexical cue
T1 8-15 DiseaseClass denotes disease
T2 21-87 SpecificDisease denotes deficiency of mitochondrial very-long-chain acyl-CoA dehydrogenase
T3 195-215 DiseaseClass denotes fatty acid oxidation
T4 309-356 SpecificDisease denotes very-long-chain acyl-CoA dehydrogenases (VLCAD)
T5 426-451 SpecificDisease denotes disease, VLCAD deficiency
T6 597-602 SpecificDisease denotes VLCAD

NCBI-Disease-Corpus-Simple-All

Id Subject Object Predicate Lexical cue
T1 8-87 SpecificDisease denotes disease with deficiency of mitochondrial very-long-chain acyl-CoA dehydrogenase
T2 350-355 SpecificDisease denotes VLCAD
T3 426-451 SpecificDisease denotes disease, VLCAD deficiency
T4 597-602 SpecificDisease denotes VLCAD