Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP446531.RAme7CQD7SG6dRxwLfl2VwrtVPNZaVdk-hGLn6D_JQY30130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP446531.RAme7CQD7SG6dRxwLfl2VwrtVPNZaVdk-hGLn6D_JQY30130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP446531.RAme7CQD7SG6dRxwLfl2VwrtVPNZaVdk-hGLn6D_JQY30130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP446531.RAme7CQD7SG6dRxwLfl2VwrtVPNZaVdk-hGLn6D_JQY30130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP446531.RAme7CQD7SG6dRxwLfl2VwrtVPNZaVdk-hGLn6D_JQY30130_provenance.