Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP844418.RA4I3zouqZ1ygnJnEoyHxiIVQOiymk2qpWj2GSr4LQbtM130_assertion> ?p ?o ?g. }
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- NP844418.RA4I3zouqZ1ygnJnEoyHxiIVQOiymk2qpWj2GSr4LQbtM130_assertion type Assertion NP844418.RA4I3zouqZ1ygnJnEoyHxiIVQOiymk2qpWj2GSr4LQbtM130_head.
- NP844418.RA4I3zouqZ1ygnJnEoyHxiIVQOiymk2qpWj2GSr4LQbtM130_assertion description "[The retinal dystrophy associated with the Pro23Ala mutation is characteristically mild in presentation and course, with greater preservation of ERG amplitudes than the more prevalent Pro23His mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP844418.RA4I3zouqZ1ygnJnEoyHxiIVQOiymk2qpWj2GSr4LQbtM130_provenance.
- NP844418.RA4I3zouqZ1ygnJnEoyHxiIVQOiymk2qpWj2GSr4LQbtM130_assertion evidence source_evidence_literature NP844418.RA4I3zouqZ1ygnJnEoyHxiIVQOiymk2qpWj2GSr4LQbtM130_provenance.
- NP844418.RA4I3zouqZ1ygnJnEoyHxiIVQOiymk2qpWj2GSr4LQbtM130_assertion SIO_000772 10980774 NP844418.RA4I3zouqZ1ygnJnEoyHxiIVQOiymk2qpWj2GSr4LQbtM130_provenance.
- NP844418.RA4I3zouqZ1ygnJnEoyHxiIVQOiymk2qpWj2GSr4LQbtM130_assertion wasDerivedFrom befree-20140225 NP844418.RA4I3zouqZ1ygnJnEoyHxiIVQOiymk2qpWj2GSr4LQbtM130_provenance.
- NP844418.RA4I3zouqZ1ygnJnEoyHxiIVQOiymk2qpWj2GSr4LQbtM130_assertion wasGeneratedBy ECO_0000203 NP844418.RA4I3zouqZ1ygnJnEoyHxiIVQOiymk2qpWj2GSr4LQbtM130_provenance.