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http://purl.uniprot.org/diseases/3327http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Disease
http://purl.uniprot.org/diseases/3327http://www.w3.org/2000/01/rdf-schema#comment"A disorder primarily characterized by craniofacial, skeletal and ectodermal abnormalities. Clinical features include craniosynostosis, narrow rib cage, short limbs, brachydactyly, hypoplastic and widely spaced teeth, sparse hair, skin laxity and abnormal nails. Nephronophthisis leading to progressive renal failure, hepatic fibrosis, heart defects, and retinitis pigmentosa have also been described."xsd:string
http://purl.uniprot.org/diseases/3327http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://purl.uniprot.org/keywords/1186
http://purl.uniprot.org/diseases/3327http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://purl.uniprot.org/keywords/38
http://purl.uniprot.org/diseases/3327http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://purl.uniprot.org/mim/614378
http://purl.uniprot.org/diseases/3327http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://id.nlm.nih.gov/mesh/D004476
http://purl.uniprot.org/diseases/3327http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://purl.uniprot.org/medgen/C3280616
http://purl.uniprot.org/diseases/3327http://www.w3.org/2004/02/skos/core#prefLabel"Cranioectodermal dysplasia 4"xsd:string
http://purl.uniprot.org/diseases/3327http://purl.uniprot.org/core/mnemonic"CED4"xsd:string
http://purl.uniprot.org/diseases/3327http://www.w3.org/2004/02/skos/core#altLabel"Sensenbrenner syndrome 4"xsd:string
http://purl.uniprot.org/uniprot/Q8NEZ3#SIPFBCF135BECF83B3Dhttp://purl.uniprot.org/core/diseasehttp://purl.uniprot.org/diseases/3327
http://purl.uniprot.org/annotation/VAR_067314http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/3327
http://purl.uniprot.org/uniprot/#_398253C1399EFAE9_up.disease_CC824F918C9C278Ehttp://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/diseases/3327