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http://purl.uniprot.org/citations/12634870http://purl.uniprot.org/core/author"Kehl H.G."xsd:string
http://purl.uniprot.org/citations/12634870http://purl.uniprot.org/core/pages"201-206"xsd:string
http://purl.uniprot.org/citations/12634870http://purl.uniprot.org/core/author"Meinecke P."xsd:string
http://purl.uniprot.org/citations/12634870http://purl.uniprot.org/core/date"2003"xsd:gYear
http://purl.uniprot.org/citations/12634870http://purl.uniprot.org/core/author"Ropers H.-H."xsd:string
http://purl.uniprot.org/citations/12634870http://purl.uniprot.org/core/author"Hoeltzenbein M."xsd:string
http://purl.uniprot.org/citations/12634870http://purl.uniprot.org/core/author"Gillessen-Kaesbach G."xsd:string
http://purl.uniprot.org/citations/12634870http://purl.uniprot.org/core/author"Schweiger S."xsd:string
http://purl.uniprot.org/citations/12634870http://purl.org/dc/terms/identifier"doi:10.1038/sj.ejhg.5200935"xsd:string
http://purl.uniprot.org/uniprot/Q06124http://purl.uniprot.org/core/citationhttp://purl.uniprot.org/citations/12634870
http://purl.uniprot.org/citations/12634870http://purl.uniprot.org/core/name"Eur. J. Hum. Genet."xsd:string
http://purl.uniprot.org/citations/12634870http://purl.uniprot.org/core/author"Hinkel G.K."xsd:string
http://purl.uniprot.org/citations/12634870http://purl.uniprot.org/core/author"Musante L."xsd:string
http://purl.uniprot.org/citations/12634870http://purl.uniprot.org/core/author"Tinschert S."xsd:string
http://purl.uniprot.org/citations/12634870http://purl.uniprot.org/core/volume"11"xsd:string
http://purl.uniprot.org/uniprot/#_Q06124-citation-12634870http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/12634870
http://purl.uniprot.org/citations/12634870http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/12634870
http://purl.uniprot.org/citations/12634870http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/12634870http://purl.uniprot.org/core/title"Spectrum of mutations in PTPN11 and genotype-phenotype correlation in 96 patients with Noonan syndrome and five patients with cardio-facio-cutaneous syndrome."xsd:string
http://purl.uniprot.org/citations/12634870http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/12634870
http://purl.uniprot.org/citations/12634870http://purl.uniprot.org/core/erratumhttp://purl.uniprot.org/citations/SIP5829902E827DEC25
http://purl.uniprot.org/citations/12634870http://purl.uniprot.org/core/author"Wieczorek D."xsd:string
http://purl.uniprot.org/citations/12634870http://purl.uniprot.org/core/author"Kalscheuer V.M."xsd:string
http://purl.uniprot.org/uniprot/Q06124#attribution-77D3B2E3FD5AA6C852A59EFE94E4E50Fhttp://purl.uniprot.org/core/sourcehttp://purl.uniprot.org/citations/12634870
http://purl.uniprot.org/citations/12634870http://purl.uniprot.org/core/author"Majewski F."xsd:string