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http://purl.uniprot.org/diseases/2106http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Disease
http://purl.uniprot.org/diseases/2106http://www.w3.org/2000/01/rdf-schema#comment"An autosomal dominant form of osteogenesis imperfecta, a connective tissue disorder characterized by low bone mass, bone fragility and susceptibility to fractures after minimal trauma. Disease severity ranges from very mild forms without fractures to intrauterine fractures and perinatal lethality. Extraskeletal manifestations, which affect a variable number of patients, are dentinogenesis imperfecta, hearing loss, and blue sclerae. OI1 is a non-deforming form with normal height or mild short stature, and no dentinogenesis imperfecta."xsd:string
http://purl.uniprot.org/diseases/2106http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://purl.uniprot.org/keywords/1065
http://purl.uniprot.org/diseases/2106http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://purl.uniprot.org/mim/166200
http://purl.uniprot.org/diseases/2106http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://id.nlm.nih.gov/mesh/D010013
http://purl.uniprot.org/diseases/2106http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://purl.uniprot.org/medgen/C0023931
http://purl.uniprot.org/diseases/2106http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://purl.uniprot.org/medgen/C2674706
http://purl.uniprot.org/diseases/2106http://www.w3.org/2004/02/skos/core#prefLabel"Osteogenesis imperfecta 1"xsd:string
http://purl.uniprot.org/diseases/2106http://purl.uniprot.org/core/mnemonic"OI1"xsd:string
http://purl.uniprot.org/diseases/2106http://www.w3.org/2004/02/skos/core#altLabel"OI, type I"xsd:string
http://purl.uniprot.org/diseases/2106http://www.w3.org/2004/02/skos/core#altLabel"OI-I"xsd:string
http://purl.uniprot.org/diseases/2106http://www.w3.org/2004/02/skos/core#altLabel"Osteogenesis imperfecta tarda"xsd:string
http://purl.uniprot.org/diseases/2106http://www.w3.org/2004/02/skos/core#altLabel"Osteogenesis imperfecta type I"xsd:string
http://purl.uniprot.org/diseases/2106http://www.w3.org/2004/02/skos/core#altLabel"Osteogenesis imperfecta with blue sclerae"xsd:string
http://purl.uniprot.org/diseases/2106http://www.w3.org/2004/02/skos/core#altLabel"Osteopenic non-fracture syndrome"xsd:string
http://purl.uniprot.org/uniprot/P02452#SIP2FBE1E2F54A4737Ahttp://purl.uniprot.org/core/diseasehttp://purl.uniprot.org/diseases/2106
http://purl.uniprot.org/uniprot/P08123#SIPF14EC8E7DC9D1BBAhttp://purl.uniprot.org/core/diseasehttp://purl.uniprot.org/diseases/2106
http://purl.uniprot.org/annotation/VAR_001644http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/2106
http://purl.uniprot.org/annotation/VAR_001645http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/2106
http://purl.uniprot.org/annotation/VAR_001646http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/2106
http://purl.uniprot.org/annotation/VAR_001647http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/2106
http://purl.uniprot.org/annotation/VAR_001648http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/2106
http://purl.uniprot.org/annotation/VAR_001714http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/2106
http://purl.uniprot.org/annotation/VAR_001731http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/2106
http://purl.uniprot.org/annotation/VAR_063292http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/2106