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http://purl.uniprot.org/citations/1496017http://purl.uniprot.org/core/author"Luthman H."xsd:string
http://purl.uniprot.org/citations/1496017http://purl.uniprot.org/core/author"Wedell A."xsd:string
http://purl.uniprot.org/citations/1496017http://purl.uniprot.org/core/volume"89"xsd:string
http://purl.uniprot.org/citations/1496017http://purl.uniprot.org/core/author"Haglund-Stengler B."xsd:string
http://purl.uniprot.org/citations/1496017http://purl.uniprot.org/core/author"Ritzen E.M."xsd:string
http://purl.uniprot.org/citations/1496017http://purl.uniprot.org/core/pages"7232-7236"xsd:string
http://purl.uniprot.org/citations/1496017http://purl.org/dc/terms/identifier"doi:10.1073/pnas.89.15.7232"xsd:string
http://purl.uniprot.org/citations/1496017http://purl.uniprot.org/core/date"1992"xsd:gYear
http://purl.uniprot.org/citations/1496017http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/1496017http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/1496017
http://purl.uniprot.org/citations/1496017http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/1496017
http://purl.uniprot.org/citations/1496017http://purl.uniprot.org/core/title"Steroid 21-hydroxylase deficiency: three additional mutated alleles and establishment of phenotype-genotype relationships of common mutations."xsd:string
http://purl.uniprot.org/uniprot/#_P08686-citation-1496017http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/1496017
http://purl.uniprot.org/uniprot/P08686#attribution-8ED29971786C5E73E872156BF70CCD8Bhttp://purl.uniprot.org/core/sourcehttp://purl.uniprot.org/citations/1496017
http://purl.uniprot.org/citations/1496017http://purl.uniprot.org/core/name"Proc. Natl. Acad. Sci. U.S.A."xsd:string
http://purl.uniprot.org/uniprot/P08686http://purl.uniprot.org/core/citationhttp://purl.uniprot.org/citations/1496017