Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP446531.RAme7CQD7SG6dRxwLfl2VwrtVPNZaVdk-hGLn6D_JQY30130_assertion> ?p ?o ?g. }
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- NP446531.RAme7CQD7SG6dRxwLfl2VwrtVPNZaVdk-hGLn6D_JQY30130_assertion type Assertion NP446531.RAme7CQD7SG6dRxwLfl2VwrtVPNZaVdk-hGLn6D_JQY30130_head.
- NP446531.RAme7CQD7SG6dRxwLfl2VwrtVPNZaVdk-hGLn6D_JQY30130_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." NP446531.RAme7CQD7SG6dRxwLfl2VwrtVPNZaVdk-hGLn6D_JQY30130_provenance.
- NP446531.RAme7CQD7SG6dRxwLfl2VwrtVPNZaVdk-hGLn6D_JQY30130_assertion evidence source_evidence_literature NP446531.RAme7CQD7SG6dRxwLfl2VwrtVPNZaVdk-hGLn6D_JQY30130_provenance.
- NP446531.RAme7CQD7SG6dRxwLfl2VwrtVPNZaVdk-hGLn6D_JQY30130_assertion SIO_000772 7795590 NP446531.RAme7CQD7SG6dRxwLfl2VwrtVPNZaVdk-hGLn6D_JQY30130_provenance.
- NP446531.RAme7CQD7SG6dRxwLfl2VwrtVPNZaVdk-hGLn6D_JQY30130_assertion wasDerivedFrom befree-20140225 NP446531.RAme7CQD7SG6dRxwLfl2VwrtVPNZaVdk-hGLn6D_JQY30130_provenance.
- NP446531.RAme7CQD7SG6dRxwLfl2VwrtVPNZaVdk-hGLn6D_JQY30130_assertion wasGeneratedBy ECO_0000203 NP446531.RAme7CQD7SG6dRxwLfl2VwrtVPNZaVdk-hGLn6D_JQY30130_provenance.