| http://purl.uniprot.org/diseases/6270 | http://www.w3.org/1999/02/22-rdf-syntax-ns#type | http://purl.uniprot.org/core/Disease |
| http://purl.uniprot.org/diseases/6270 | http://www.w3.org/2000/01/rdf-schema#comment | "A form of retinitis pigmentosa, a retinal dystrophy belonging to the group of pigmentary retinopathies. Retinitis pigmentosa is characterized by retinal pigment deposits visible on fundus examination and primary loss of rod photoreceptor cells followed by secondary loss of cone photoreceptors. Patients typically have night vision blindness and loss of midperipheral visual field. RP92 is an autosomal recessive, mild form with onset of night blindness and vision loss in the third to sixth decades of life."xsd:string |
| http://purl.uniprot.org/diseases/6270 | http://www.w3.org/2000/01/rdf-schema#seeAlso | http://purl.uniprot.org/keywords/682 |
| http://purl.uniprot.org/diseases/6270 | http://www.w3.org/2000/01/rdf-schema#seeAlso | http://purl.uniprot.org/mim/619614 |
| http://purl.uniprot.org/diseases/6270 | http://www.w3.org/2000/01/rdf-schema#seeAlso | http://id.nlm.nih.gov/mesh/D012174 |
| http://purl.uniprot.org/diseases/6270 | http://www.w3.org/2000/01/rdf-schema#seeAlso | http://purl.uniprot.org/medgen/CN301253 |
| http://purl.uniprot.org/diseases/6270 | http://www.w3.org/2004/02/skos/core#prefLabel | "Retinitis pigmentosa 92"xsd:string |
| http://purl.uniprot.org/diseases/6270 | http://purl.uniprot.org/core/mnemonic | "RP92"xsd:string |
| http://purl.uniprot.org/uniprot/Q2TB90#SIPA05971F965C8F266 | http://purl.uniprot.org/core/disease | http://purl.uniprot.org/diseases/6270 |
| http://purl.uniprot.org/annotation/VAR_086465 | http://www.w3.org/2004/02/skos/core#related | http://purl.uniprot.org/diseases/6270 |
| http://purl.uniprot.org/uniprot/#_3606C92CD1106545_up.disease_4BBAAD93353EB746 | http://www.w3.org/1999/02/22-rdf-syntax-ns#object | http://purl.uniprot.org/diseases/6270 |