Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP456135.RAqtoTsFFmtjEdaR-napfK0M-XbZs37S8RP7uZGHhQtn8130_assertion> ?p ?o ?g. }
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- NP456135.RAqtoTsFFmtjEdaR-napfK0M-XbZs37S8RP7uZGHhQtn8130_assertion type Assertion NP456135.RAqtoTsFFmtjEdaR-napfK0M-XbZs37S8RP7uZGHhQtn8130_head.
- NP456135.RAqtoTsFFmtjEdaR-napfK0M-XbZs37S8RP7uZGHhQtn8130_assertion description "[Ocular albinism type 1 (OA1) is an X-linked recessive disorder characterized by a major impairment of visual acuity, nystagmus, strabismus, photophobia and retinal hypopigmentation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP456135.RAqtoTsFFmtjEdaR-napfK0M-XbZs37S8RP7uZGHhQtn8130_provenance.
- NP456135.RAqtoTsFFmtjEdaR-napfK0M-XbZs37S8RP7uZGHhQtn8130_assertion evidence source_evidence_literature NP456135.RAqtoTsFFmtjEdaR-napfK0M-XbZs37S8RP7uZGHhQtn8130_provenance.
- NP456135.RAqtoTsFFmtjEdaR-napfK0M-XbZs37S8RP7uZGHhQtn8130_assertion SIO_000772 7795590 NP456135.RAqtoTsFFmtjEdaR-napfK0M-XbZs37S8RP7uZGHhQtn8130_provenance.
- NP456135.RAqtoTsFFmtjEdaR-napfK0M-XbZs37S8RP7uZGHhQtn8130_assertion wasDerivedFrom befree-20140225 NP456135.RAqtoTsFFmtjEdaR-napfK0M-XbZs37S8RP7uZGHhQtn8130_provenance.
- NP456135.RAqtoTsFFmtjEdaR-napfK0M-XbZs37S8RP7uZGHhQtn8130_assertion wasGeneratedBy ECO_0000203 NP456135.RAqtoTsFFmtjEdaR-napfK0M-XbZs37S8RP7uZGHhQtn8130_provenance.