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PubMed:21943124 / 0-152 JSONTXT

Annnotations TAB JSON ListView MergeView

sentences

Id Subject Object Predicate Lexical cue
TextSentencer_T1 0-86 Sentence denotes A deletion of FGFR2 creating a chimeric IIIb/IIIc exon in a child with Apert syndrome.
TextSentencer_T2 87-98 Sentence denotes BACKGROUND:
T1 0-86 Sentence denotes A deletion of FGFR2 creating a chimeric IIIb/IIIc exon in a child with Apert syndrome.
T2 87-98 Sentence denotes BACKGROUND:

DisGeNET

Id Subject Object Predicate Lexical cue
T0 14-19 gene:2263 denotes FGFR2
T1 71-85 disease:C0001193 denotes Apert syndrome
R1 T0 T1 associated_with FGFR2,Apert syndrome

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
21943124-0#14#19#gene2263 14-19 gene2263 denotes FGFR2
21943124-0#71#85#diseaseC0001193 71-85 diseaseC0001193 denotes Apert syndrome
14#19#gene226371#85#diseaseC0001193 21943124-0#14#19#gene2263 21943124-0#71#85#diseaseC0001193 associated_with FGFR2,Apert syndrome

PubCasesORDO

Id Subject Object Predicate Lexical cue
TI1 71-85 ORDO:87 denotes Apert syndrome