Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP246685.RAAijAk6HXCLzpJxow__ZljrRXNXEdt_EdTKNVVaRDCps130_assertion> ?p ?o ?g. }
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- NP246685.RAAijAk6HXCLzpJxow__ZljrRXNXEdt_EdTKNVVaRDCps130_assertion type Assertion NP246685.RAAijAk6HXCLzpJxow__ZljrRXNXEdt_EdTKNVVaRDCps130_head.
- NP246685.RAAijAk6HXCLzpJxow__ZljrRXNXEdt_EdTKNVVaRDCps130_assertion description "[Functional analysis of human CNGA3 mutations associated with colour blindness suggests impaired surface expression of channel mutants A3(R427C) and A3(R563C).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP246685.RAAijAk6HXCLzpJxow__ZljrRXNXEdt_EdTKNVVaRDCps130_provenance.
- NP246685.RAAijAk6HXCLzpJxow__ZljrRXNXEdt_EdTKNVVaRDCps130_assertion evidence source_evidence_literature NP246685.RAAijAk6HXCLzpJxow__ZljrRXNXEdt_EdTKNVVaRDCps130_provenance.
- NP246685.RAAijAk6HXCLzpJxow__ZljrRXNXEdt_EdTKNVVaRDCps130_assertion SIO_000772 18445228 NP246685.RAAijAk6HXCLzpJxow__ZljrRXNXEdt_EdTKNVVaRDCps130_provenance.
- NP246685.RAAijAk6HXCLzpJxow__ZljrRXNXEdt_EdTKNVVaRDCps130_assertion wasDerivedFrom befree-20140225 NP246685.RAAijAk6HXCLzpJxow__ZljrRXNXEdt_EdTKNVVaRDCps130_provenance.
- NP246685.RAAijAk6HXCLzpJxow__ZljrRXNXEdt_EdTKNVVaRDCps130_assertion wasGeneratedBy ECO_0000203 NP246685.RAAijAk6HXCLzpJxow__ZljrRXNXEdt_EdTKNVVaRDCps130_provenance.