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SubjectPredicateObject
http://purl.uniprot.org/citations/22344793http://purl.uniprot.org/core/author"Antinolo G."xsd:string
http://purl.uniprot.org/citations/22344793http://purl.uniprot.org/core/pages"816-820"xsd:string
http://purl.uniprot.org/citations/22344793http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/22344793
http://purl.uniprot.org/uniprot/#_P32004-citation-22344793http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/22344793
http://purl.uniprot.org/uniprot/P32004http://purl.uniprot.org/core/citationhttp://purl.uniprot.org/citations/22344793
http://purl.uniprot.org/citations/22344793http://purl.uniprot.org/core/author"Borrego S."xsd:string
http://purl.uniprot.org/citations/22344793http://purl.uniprot.org/core/name"Am. J. Med. Genet. A"xsd:string
http://purl.uniprot.org/citations/22344793http://purl.uniprot.org/core/author"Nunez-Torres R."xsd:string
http://purl.uniprot.org/citations/22344793http://purl.uniprot.org/core/volume"158"xsd:string
http://purl.uniprot.org/citations/22344793http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/22344793
http://purl.uniprot.org/citations/22344793http://purl.uniprot.org/core/date"2012"xsd:gYear
http://purl.uniprot.org/uniprot/P32004#attribution-1AD7562362CFD73D885560767570F57Dhttp://purl.uniprot.org/core/sourcehttp://purl.uniprot.org/citations/22344793
http://purl.uniprot.org/citations/22344793http://purl.uniprot.org/core/author"de Agustin J.C."xsd:string
http://purl.uniprot.org/citations/22344793http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/22344793http://purl.uniprot.org/core/author"Fernandez R.M."xsd:string
http://purl.uniprot.org/citations/22344793http://purl.uniprot.org/core/author"Garcia-Diaz L."xsd:string
http://purl.uniprot.org/citations/22344793http://purl.org/dc/terms/identifier"doi:10.1002/ajmg.a.35244"xsd:string
http://purl.uniprot.org/citations/22344793http://purl.uniprot.org/core/title"Association of X-linked hydrocephalus and Hirschsprung disease: Report of a new patient with a mutation in the L1CAM gene."xsd:string