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PubMed:2404853 JSONTXT

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sentences

Id Subject Object Predicate Lexical cue
TextSentencer_T1 0-73 Sentence denotes A normal male with an inherited deletion of one exon within the DMD gene.
TextSentencer_T2 74-302 Sentence denotes We describe two brothers with identical inherited deletions of one single exon within the middle of the DMD gene; one brother has Becker muscular dystrophy diagnosed at 11 years of age, whereas the older brother is normal at 18.
TextSentencer_T3 303-425 Sentence denotes These results have implications for genetic counselling and prenatal diagnosis in families with Becker muscular dystrophy.
T1 0-73 Sentence denotes A normal male with an inherited deletion of one exon within the DMD gene.
T2 74-302 Sentence denotes We describe two brothers with identical inherited deletions of one single exon within the middle of the DMD gene; one brother has Becker muscular dystrophy diagnosed at 11 years of age, whereas the older brother is normal at 18.
T3 303-425 Sentence denotes These results have implications for genetic counselling and prenatal diagnosis in families with Becker muscular dystrophy.

DisGeNET

Id Subject Object Predicate Lexical cue
T0 178-181 gene:1756 denotes DMD
T1 204-229 disease:C0917713 denotes Becker muscular dystrophy
R1 T0 T1 associated_with DMD,Becker muscular dystrophy

PubmedHPO

Id Subject Object Predicate Lexical cue
T1 211-229 HP_0003560 denotes muscular dystrophy
T2 406-424 HP_0003560 denotes muscular dystrophy

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
2404853-1#104#107#gene1756 178-181 gene1756 denotes DMD
2404853-1#130#155#diseaseC0917713 204-229 diseaseC0917713 denotes Becker muscular dystrophy
104#107#gene1756130#155#diseaseC0917713 2404853-1#104#107#gene1756 2404853-1#130#155#diseaseC0917713 associated_with DMD,Becker muscular dystrophy

PubCasesHPO

Id Subject Object Predicate Lexical cue
AB1 211-229 HP:0003560 denotes muscular dystrophy
AB2 406-424 HP:0003560 denotes muscular dystrophy

PubCasesORDO

Id Subject Object Predicate Lexical cue
AB1 204-229 ORDO:98895 denotes Becker muscular dystrophy
AB2 399-424 ORDO:98895 denotes Becker muscular dystrophy

NCBIDiseaseCorpus

Id Subject Object Predicate Lexical cue
T1 64-67 Modifier:D020388 denotes DMD
T2 178-181 Modifier:D020388 denotes DMD
T3 204-229 SpecificDisease:C537666 denotes Becker muscular dystrophy
T4 399-424 SpecificDisease:C537666 denotes Becker muscular dystrophy

NCBI-Disease-Train

Id Subject Object Predicate Lexical cue database_id
T1726 64-67 Modifier denotes DMD D020388
T1727 178-181 Modifier denotes DMD D020388
T1728 204-229 SpecificDisease denotes Becker muscular dystrophy C537666
T1729 399-424 SpecificDisease denotes Becker muscular dystrophy C537666

NCBI-Disease-Corpus-All

Id Subject Object Predicate Lexical cue database_id
T1726 64-67 Modifier denotes DMD D020388
T1727 178-181 Modifier denotes DMD D020388
T1728 204-229 SpecificDisease denotes Becker muscular dystrophy C537666
T1729 399-424 SpecificDisease denotes Becker muscular dystrophy C537666

NCBI-Disease-Corpus-2stage-All

Id Subject Object Predicate Lexical cue
T1 204-229 SpecificDisease denotes Becker muscular dystrophy
T2 399-424 SpecificDisease denotes Becker muscular dystrophy

NCBI-Disease-Corpus-rezarta-All

Id Subject Object Predicate Lexical cue
T1 204-229 SpecificDisease denotes Becker muscular dystrophy
T2 399-424 SpecificDisease denotes Becker muscular dystrophy

NCBI-Disease-Corpus-4oGuideline-All

Id Subject Object Predicate Lexical cue
T1 204-229 SpecificDisease denotes Becker muscular dystrophy
T2 399-424 SpecificDisease denotes Becker muscular dystrophy

NCBI-Disease-Corpus-Simple-All

Id Subject Object Predicate Lexical cue
T1 204-229 SpecificDisease denotes Becker muscular dystrophy
T2 399-424 SpecificDisease denotes Becker muscular dystrophy