Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP714427.RAx96TpJAIKbNQW_t_hOLg72WYKt4f64AIokuHX8JwoGY130_assertion> ?p ?o ?g. }
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- NP714427.RAx96TpJAIKbNQW_t_hOLg72WYKt4f64AIokuHX8JwoGY130_assertion type Assertion NP714427.RAx96TpJAIKbNQW_t_hOLg72WYKt4f64AIokuHX8JwoGY130_head.
- NP714427.RAx96TpJAIKbNQW_t_hOLg72WYKt4f64AIokuHX8JwoGY130_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." NP714427.RAx96TpJAIKbNQW_t_hOLg72WYKt4f64AIokuHX8JwoGY130_provenance.
- NP714427.RAx96TpJAIKbNQW_t_hOLg72WYKt4f64AIokuHX8JwoGY130_assertion evidence source_evidence_literature NP714427.RAx96TpJAIKbNQW_t_hOLg72WYKt4f64AIokuHX8JwoGY130_provenance.
- NP714427.RAx96TpJAIKbNQW_t_hOLg72WYKt4f64AIokuHX8JwoGY130_assertion SIO_000772 10581037 NP714427.RAx96TpJAIKbNQW_t_hOLg72WYKt4f64AIokuHX8JwoGY130_provenance.
- NP714427.RAx96TpJAIKbNQW_t_hOLg72WYKt4f64AIokuHX8JwoGY130_assertion wasDerivedFrom befree-20140225 NP714427.RAx96TpJAIKbNQW_t_hOLg72WYKt4f64AIokuHX8JwoGY130_provenance.
- NP714427.RAx96TpJAIKbNQW_t_hOLg72WYKt4f64AIokuHX8JwoGY130_assertion wasGeneratedBy ECO_0000203 NP714427.RAx96TpJAIKbNQW_t_hOLg72WYKt4f64AIokuHX8JwoGY130_provenance.