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http://purl.uniprot.org/keywords/586http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Concept
http://purl.uniprot.org/keywords/586http://www.w3.org/2000/01/rdf-schema#subClassOfhttp://purl.uniprot.org/core/Concept
http://purl.uniprot.org/keywords/586http://www.w3.org/2000/01/rdf-schema#subClassOfhttp://purl.uniprot.org/keywords/9995
http://purl.uniprot.org/keywords/586http://www.w3.org/2000/01/rdf-schema#comment"Protein which, if defective, causes phenylketonuria, an autosomal recessive disorder in which the body is unable to break down the amino acid phenylalanine. The resulting buildup of phenylalanine in the body causes intellectual disability, mental disturbances, eczema and skin pigmentation."xsd:string
http://purl.uniprot.org/keywords/586http://www.w3.org/2004/02/skos/core#prefLabel"Phenylketonuria"xsd:string
http://purl.uniprot.org/keywords/586http://purl.uniprot.org/core/categoryhttp://purl.uniprot.org/keywords/9995
http://purl.uniprot.org/uniprot/P09417http://purl.uniprot.org/core/classifiedWithhttp://purl.uniprot.org/keywords/586
http://purl.uniprot.org/uniprot/P30793http://purl.uniprot.org/core/classifiedWithhttp://purl.uniprot.org/keywords/586
http://purl.uniprot.org/uniprot/Q03393http://purl.uniprot.org/core/classifiedWithhttp://purl.uniprot.org/keywords/586
http://purl.uniprot.org/uniprot/P00439http://purl.uniprot.org/core/classifiedWithhttp://purl.uniprot.org/keywords/586
http://purl.uniprot.org/uniprot/P27213http://purl.uniprot.org/core/classifiedWithhttp://purl.uniprot.org/keywords/586
http://purl.uniprot.org/keywords/9995http://www.w3.org/2004/02/skos/core#narrowerhttp://purl.uniprot.org/keywords/586