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http://purl.uniprot.org/diseases/2088http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Disease
http://purl.uniprot.org/diseases/2088http://www.w3.org/2000/01/rdf-schema#comment"An autosomal recessive disorder in which the biosynthesis of melanin pigment is absent in skin, hair, and eyes. It is characterized by complete lack of tyrosinase activity due to production of an inactive enzyme. Patients present with a life-long absence of melanin pigment after birth, and manifest increased sensitivity to ultraviolet radiation with predisposition to skin cancer. Visual anomalies include decreased acuity, nystagmus, strabismus and photophobia."xsd:string
http://purl.uniprot.org/diseases/2088http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://purl.uniprot.org/keywords/15
http://purl.uniprot.org/diseases/2088http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://purl.uniprot.org/mim/203100
http://purl.uniprot.org/diseases/2088http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://id.nlm.nih.gov/mesh/D016115
http://purl.uniprot.org/diseases/2088http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://purl.uniprot.org/medgen/C0268494
http://purl.uniprot.org/diseases/2088http://www.w3.org/2004/02/skos/core#prefLabel"Albinism, oculocutaneous, 1A"xsd:string
http://purl.uniprot.org/diseases/2088http://purl.uniprot.org/core/mnemonic"OCA1A"xsd:string
http://purl.uniprot.org/diseases/2088http://www.w3.org/2004/02/skos/core#altLabel"ATN"xsd:string
http://purl.uniprot.org/diseases/2088http://www.w3.org/2004/02/skos/core#altLabel"Albinism I"xsd:string
http://purl.uniprot.org/diseases/2088http://www.w3.org/2004/02/skos/core#altLabel"Albinism oculocutaneous IA"xsd:string
http://purl.uniprot.org/diseases/2088http://www.w3.org/2004/02/skos/core#altLabel"OCA-1A"xsd:string
http://purl.uniprot.org/diseases/2088http://www.w3.org/2004/02/skos/core#altLabel"OCA-IA"xsd:string
http://purl.uniprot.org/diseases/2088http://www.w3.org/2004/02/skos/core#altLabel"Oculocutaneous albinism tyrosinase negative"xsd:string
http://purl.uniprot.org/uniprot/P14679#SIP1110A09D1099F6C1http://purl.uniprot.org/core/diseasehttp://purl.uniprot.org/diseases/2088
http://purl.uniprot.org/annotation/VAR_007649http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/2088
http://purl.uniprot.org/annotation/VAR_007650http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/2088
http://purl.uniprot.org/annotation/VAR_007651http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/2088
http://purl.uniprot.org/annotation/VAR_007652http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/2088
http://purl.uniprot.org/annotation/VAR_007654http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/2088
http://purl.uniprot.org/annotation/VAR_007655http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/2088
http://purl.uniprot.org/annotation/VAR_007656http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/2088
http://purl.uniprot.org/annotation/VAR_007657http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/2088
http://purl.uniprot.org/annotation/VAR_007658http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/2088
http://purl.uniprot.org/annotation/VAR_007659http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/2088