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PubMed:24123776 / 461-670 JSONTXT

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sentences

Id Subject Object Predicate Lexical cue
TextSentencer_T4 0-209 Sentence denotes We review 39 patients including two new patients, one with compound heterozygous novel mutations in WDR35 and a previously unreported multisutural craniosynostosis that may be a part of Sensenbrenner syndrome.
T4 0-209 Sentence denotes We review 39 patients including two new patients, one with compound heterozygous novel mutations in WDR35 and a previously unreported multisutural craniosynostosis that may be a part of Sensenbrenner syndrome.

DisGeNET

Id Subject Object Predicate Lexical cue
T0 100-105 gene:57539 denotes WDR35
T1 186-208 disease:C0432235 denotes Sensenbrenner syndrome
T2 100-105 gene:57539 denotes WDR35
T3 147-163 disease:C0010278 denotes craniosynostosis
R1 T0 T1 associated_with WDR35,Sensenbrenner syndrome
R2 T2 T3 associated_with WDR35,craniosynostosis

PubmedHPO

Id Subject Object Predicate Lexical cue
T2 134-163 HP_0011324 denotes multisutural craniosynostosis
T3 147-163 HP_0001363 denotes craniosynostosis

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
24123776-3#100#105#gene57539 100-105 gene57539 denotes WDR35
24123776-3#147#163#diseaseC0010278 147-163 diseaseC0010278 denotes craniosynostosis
24123776-3#186#208#diseaseC0432235 186-208 diseaseC0432235 denotes Sensenbrenner syndrome
100#105#gene57539147#163#diseaseC0010278 24123776-3#100#105#gene57539 24123776-3#147#163#diseaseC0010278 associated_with WDR35,craniosynostosis
100#105#gene57539186#208#diseaseC0432235 24123776-3#100#105#gene57539 24123776-3#186#208#diseaseC0432235 associated_with WDR35,Sensenbrenner syndrome

PubCasesHPO

Id Subject Object Predicate Lexical cue
AB1 147-163 HP:0001363 denotes craniosynostosis

PubCasesORDO

Id Subject Object Predicate Lexical cue
AB3 186-208 ORDO:1515 denotes Sensenbrenner syndrome