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http://purl.uniprot.org/diseases/2089http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Disease
http://purl.uniprot.org/diseases/2089http://www.w3.org/2000/01/rdf-schema#comment"An autosomal recessive disorder in which the biosynthesis of melanin pigment is reduced in skin, hair, and eyes. It is characterized by partial lack of tyrosinase activity. Patients have white hair at birth that rapidly turns yellow or blond. They manifest the development of minimal-to-moderate amounts of cutaneous and ocular pigment. Some patients may have with white hair in the warmer areas (scalp and axilla) and progressively darker hair in the cooler areas (extremities). This variant phenotype is due to a loss of tyrosinase activity above 35-37 degrees C."xsd:string
http://purl.uniprot.org/diseases/2089http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://purl.uniprot.org/keywords/15
http://purl.uniprot.org/diseases/2089http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://purl.uniprot.org/mim/606952
http://purl.uniprot.org/diseases/2089http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://id.nlm.nih.gov/mesh/D016115
http://purl.uniprot.org/diseases/2089http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://purl.uniprot.org/medgen/C1847024
http://purl.uniprot.org/diseases/2089http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://purl.uniprot.org/medgen/C1847132
http://purl.uniprot.org/diseases/2089http://www.w3.org/2004/02/skos/core#prefLabel"Albinism, oculocutaneous, 1B"xsd:string
http://purl.uniprot.org/diseases/2089http://purl.uniprot.org/core/mnemonic"OCA1B"xsd:string
http://purl.uniprot.org/diseases/2089http://www.w3.org/2004/02/skos/core#altLabel"Albinism yellow mutant type"xsd:string
http://purl.uniprot.org/diseases/2089http://www.w3.org/2004/02/skos/core#altLabel"OCA-IB"xsd:string
http://purl.uniprot.org/diseases/2089http://www.w3.org/2004/02/skos/core#altLabel"OCA-ITS"xsd:string
http://purl.uniprot.org/diseases/2089http://www.w3.org/2004/02/skos/core#altLabel"Oculocutaneous albinism type IB"xsd:string
http://purl.uniprot.org/diseases/2089http://www.w3.org/2004/02/skos/core#altLabel"Yellow albinism"xsd:string
http://purl.uniprot.org/diseases/2089http://www.w3.org/2004/02/skos/core#altLabel"Oculocutaneous albinism type I temperature-sensitive"xsd:string
http://purl.uniprot.org/uniprot/P14679#SIPC947491605FC4E38http://purl.uniprot.org/core/diseasehttp://purl.uniprot.org/diseases/2089
http://purl.uniprot.org/annotation/VAR_007669http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/2089
http://purl.uniprot.org/annotation/VAR_007675http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/2089
http://purl.uniprot.org/annotation/VAR_007681http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/2089
http://purl.uniprot.org/annotation/VAR_007684http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/2089
http://purl.uniprot.org/annotation/VAR_007687http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/2089
http://purl.uniprot.org/annotation/VAR_007689http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/2089
http://purl.uniprot.org/annotation/VAR_007691http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/2089
http://purl.uniprot.org/annotation/VAR_007925http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/2089
http://purl.uniprot.org/annotation/VAR_007928http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/2089