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http://purl.uniprot.org/citations/27868344http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/27868344http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/27868344http://purl.org/dc/terms/identifier"doi:10.1002/ajmg.a.38056"xsd:string
http://purl.uniprot.org/citations/27868344http://purl.org/dc/terms/identifier"doi:10.1002/ajmg.a.38056"xsd:string
http://purl.uniprot.org/citations/27868344http://purl.uniprot.org/core/author"Vargas A."xsd:string
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http://purl.uniprot.org/citations/27868344http://purl.uniprot.org/core/author"Marble M."xsd:string
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http://purl.uniprot.org/citations/27868344http://purl.uniprot.org/core/author"Lacassie Y."xsd:string
http://purl.uniprot.org/citations/27868344http://purl.uniprot.org/core/author"Lacassie Y."xsd:string
http://purl.uniprot.org/citations/27868344http://purl.uniprot.org/core/author"Chalew S.A."xsd:string
http://purl.uniprot.org/citations/27868344http://purl.uniprot.org/core/author"Chalew S.A."xsd:string
http://purl.uniprot.org/citations/27868344http://purl.uniprot.org/core/author"Lilje C."xsd:string
http://purl.uniprot.org/citations/27868344http://purl.uniprot.org/core/author"Lilje C."xsd:string
http://purl.uniprot.org/citations/27868344http://purl.uniprot.org/core/author"Zambrano R.M."xsd:string
http://purl.uniprot.org/citations/27868344http://purl.uniprot.org/core/author"Zambrano R.M."xsd:string
http://purl.uniprot.org/citations/27868344http://purl.uniprot.org/core/date"2017"xsd:gYear
http://purl.uniprot.org/citations/27868344http://purl.uniprot.org/core/date"2017"xsd:gYear
http://purl.uniprot.org/citations/27868344http://purl.uniprot.org/core/name"Am. J. Med. Genet. A"xsd:string
http://purl.uniprot.org/citations/27868344http://purl.uniprot.org/core/name"Am. J. Med. Genet. A"xsd:string
http://purl.uniprot.org/citations/27868344http://purl.uniprot.org/core/pages"565-567"xsd:string
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http://purl.uniprot.org/citations/27868344http://purl.uniprot.org/core/title"Further evidence that variants in PPP1CB cause a rasopathy similar to Noonan syndrome with loose anagen hair."xsd:string
http://purl.uniprot.org/citations/27868344http://purl.uniprot.org/core/title"Further evidence that variants in PPP1CB cause a rasopathy similar to Noonan syndrome with loose anagen hair."xsd:string
http://purl.uniprot.org/citations/27868344http://purl.uniprot.org/core/volume"173"xsd:string