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PubMed:2569949 / 0-93 JSONTXT

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DisGeNet-2017-sample

Id Subject Object Predicate Lexical cue
T580 26-51 gene:5053 denotes phenylalanine hydroxylase
T581 68-83 disease:C0031485 denotes phenylketonuria
R1 T580 T581 associated_with phenylalanine hydroxylase,phenylketonuria
R2 T580 T581 associated_with phenylalanine hydroxylase,phenylketonuria

sentences

Id Subject Object Predicate Lexical cue
TextSentencer_T1 0-93 Sentence denotes Haplotype analysis of the phenylalanine hydroxylase gene in Turkish phenylketonuria families.
T1 0-93 Sentence denotes Haplotype analysis of the phenylalanine hydroxylase gene in Turkish phenylketonuria families.

NCBIDiseaseCorpus

Id Subject Object Predicate Lexical cue
T1 68-83 Modifier:D010661 denotes phenylketonuria

NCBI-Disease-Train

Id Subject Object Predicate Lexical cue database_id
T2991 68-83 Modifier denotes phenylketonuria D010661

NCBI-Disease-Corpus-All

Id Subject Object Predicate Lexical cue database_id
T2991 68-83 Modifier denotes phenylketonuria D010661

NCBI-Disease-Corpus-2stage-All

Id Subject Object Predicate Lexical cue
T1 68-83 Modifier denotes phenylketonuria

NCBI-Disease-Corpus-rezarta-All

Id Subject Object Predicate Lexical cue
T1 68-83 Modifier denotes phenylketonuria

NCBI-Disease-Corpus-4oGuideline-All

Id Subject Object Predicate Lexical cue
T1 68-83 SpecificDisease denotes phenylketonuria

NCBI-Disease-Corpus-Simple-All

Id Subject Object Predicate Lexical cue
T1 68-83 SpecificDisease denotes phenylketonuria