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SubjectPredicateObject
http://purl.uniprot.org/citations/8556302http://purl.uniprot.org/core/author"van Camp G."xsd:string
http://purl.uniprot.org/citations/8556302http://purl.uniprot.org/core/author"Coucke P."xsd:string
http://purl.uniprot.org/citations/8556302http://purl.uniprot.org/core/erratumhttp://purl.uniprot.org/citations/SIP2CBA59379705FB08
http://purl.uniprot.org/citations/8556302http://purl.org/dc/terms/identifier"doi:10.1159/000472311"xsd:string
http://purl.uniprot.org/citations/8556302http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/8556302
http://purl.uniprot.org/citations/8556302http://purl.uniprot.org/core/date"1995"xsd:gYear
http://purl.uniprot.org/citations/8556302http://purl.uniprot.org/core/author"Fransen E."xsd:string
http://purl.uniprot.org/citations/8556302http://purl.uniprot.org/core/author"Willems P.J."xsd:string
http://purl.uniprot.org/citations/8556302http://purl.uniprot.org/core/author"Lemmon V."xsd:string
http://purl.uniprot.org/citations/8556302http://purl.uniprot.org/core/author"Vits L."xsd:string
http://purl.uniprot.org/uniprot/#_P32004-citation-8556302http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/8556302
http://purl.uniprot.org/citations/8556302http://purl.uniprot.org/core/pages"273-284"xsd:string
http://purl.uniprot.org/uniprot/P32004#attribution-55F439E43EAD28B335257B4E818B4898http://purl.uniprot.org/core/sourcehttp://purl.uniprot.org/citations/8556302
http://purl.uniprot.org/citations/8556302http://purl.uniprot.org/core/name"Eur. J. Hum. Genet."xsd:string
http://purl.uniprot.org/uniprot/P32004http://purl.uniprot.org/core/citationhttp://purl.uniprot.org/citations/8556302
http://purl.uniprot.org/citations/8556302http://purl.uniprot.org/core/volume"3"xsd:string
http://purl.uniprot.org/citations/8556302http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/8556302http://purl.uniprot.org/core/title"CRASH syndrome: clinical spectrum of corpus callosum hypoplasia, retardation, adducted thumbs, spastic paraparesis and hydrocephalus due to mutations in one single gene, L1."xsd:string
http://purl.uniprot.org/citations/8556302http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/8556302