Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP755853.RAdp267jaYnkAPi7tdtlClctD1hLZ1OSRuYEs-u5E7_v8130_assertion> ?p ?o ?g. }
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- NP755853.RAdp267jaYnkAPi7tdtlClctD1hLZ1OSRuYEs-u5E7_v8130_assertion type Assertion NP755853.RAdp267jaYnkAPi7tdtlClctD1hLZ1OSRuYEs-u5E7_v8130_head.
- NP755853.RAdp267jaYnkAPi7tdtlClctD1hLZ1OSRuYEs-u5E7_v8130_assertion description "[Mutations in human CRX are associated with the retinal diseases, cone-rod dystrophy-2 (adCRD2; refs 3, 4, 5), retinitis pigmentosa (RP) and Leber congenital amaurosis (LCA), which all lead to loss of vision.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP755853.RAdp267jaYnkAPi7tdtlClctD1hLZ1OSRuYEs-u5E7_v8130_provenance.
- NP755853.RAdp267jaYnkAPi7tdtlClctD1hLZ1OSRuYEs-u5E7_v8130_assertion evidence source_evidence_literature NP755853.RAdp267jaYnkAPi7tdtlClctD1hLZ1OSRuYEs-u5E7_v8130_provenance.
- NP755853.RAdp267jaYnkAPi7tdtlClctD1hLZ1OSRuYEs-u5E7_v8130_assertion SIO_000772 10581037 NP755853.RAdp267jaYnkAPi7tdtlClctD1hLZ1OSRuYEs-u5E7_v8130_provenance.
- NP755853.RAdp267jaYnkAPi7tdtlClctD1hLZ1OSRuYEs-u5E7_v8130_assertion wasDerivedFrom befree-20140225 NP755853.RAdp267jaYnkAPi7tdtlClctD1hLZ1OSRuYEs-u5E7_v8130_provenance.
- NP755853.RAdp267jaYnkAPi7tdtlClctD1hLZ1OSRuYEs-u5E7_v8130_assertion wasGeneratedBy ECO_0000203 NP755853.RAdp267jaYnkAPi7tdtlClctD1hLZ1OSRuYEs-u5E7_v8130_provenance.