PubMed:24123776 / 461-670 JSONTXT

{"project":"sentences","denotations":[{"id":"TextSentencer_T4","span":{"begin":0,"end":209},"obj":"Sentence"},{"id":"T4","span":{"begin":0,"end":209},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"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."}

{"project":"DisGeNET","denotations":[{"id":"T0","span":{"begin":100,"end":105},"obj":"gene:57539"},{"id":"T1","span":{"begin":186,"end":208},"obj":"disease:C0432235"},{"id":"T2","span":{"begin":100,"end":105},"obj":"gene:57539"},{"id":"T3","span":{"begin":147,"end":163},"obj":"disease:C0010278"}],"relations":[{"id":"R1","pred":"associated_with","subj":"T0","obj":"T1"},{"id":"R2","pred":"associated_with","subj":"T2","obj":"T3"}],"namespaces":[{"prefix":"gene","uri":"http://www.ncbi.nlm.nih.gov/gene/"},{"prefix":"disease","uri":"http://purl.bioontology.org/ontology/MEDLINEPLUS/"}],"text":"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."}

{"project":"PubmedHPO","denotations":[{"id":"T2","span":{"begin":134,"end":163},"obj":"HP_0011324"},{"id":"T3","span":{"begin":147,"end":163},"obj":"HP_0001363"}],"text":"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."}

{"project":"DisGeNET5_gene_disease","denotations":[{"id":"24123776-3#100#105#gene57539","span":{"begin":100,"end":105},"obj":"gene57539"},{"id":"24123776-3#147#163#diseaseC0010278","span":{"begin":147,"end":163},"obj":"diseaseC0010278"},{"id":"24123776-3#186#208#diseaseC0432235","span":{"begin":186,"end":208},"obj":"diseaseC0432235"}],"relations":[{"id":"100#105#gene57539147#163#diseaseC0010278","pred":"associated_with","subj":"24123776-3#100#105#gene57539","obj":"24123776-3#147#163#diseaseC0010278"},{"id":"100#105#gene57539186#208#diseaseC0432235","pred":"associated_with","subj":"24123776-3#100#105#gene57539","obj":"24123776-3#186#208#diseaseC0432235"}],"text":"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."}

{"project":"PubCasesHPO","denotations":[{"id":"AB1","span":{"begin":147,"end":163},"obj":"HP:0001363"}],"text":"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."}

{"project":"PubCasesORDO","denotations":[{"id":"AB3","span":{"begin":186,"end":208},"obj":"ORDO:1515"}],"namespaces":[{"prefix":"ORDO","uri":"http://www.orpha.net/ORDO/Orphanet_"}],"text":"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."}