Matches in Nanopublications for { ?s ?p "[Mutations in LCA5 are a rare cause of childhood retinal dystrophy accounting for ?2% of disease in this cohort, and the majority of LCA5 mutations are likely null.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 3 of
3
with 100 items per page.
- assertion description "[Mutations in LCA5 are a rare cause of childhood retinal dystrophy accounting for ?2% of disease in this cohort, and the majority of LCA5 mutations are likely null.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1102524.RAfuYOmKn09hl7kPlQwnPSh9uslPTRePpd45punUw-0Rg130_assertion description "[Mutations in LCA5 are a rare cause of childhood retinal dystrophy accounting for ?2% of disease in this cohort, and the majority of LCA5 mutations are likely null.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1102524.RAfuYOmKn09hl7kPlQwnPSh9uslPTRePpd45punUw-0Rg130_provenance.
- NP977711.RA6DrdXk20O2p7GITbGmdxV_kXF3AEKQPqt17Ts0nxqi0130_assertion description "[Mutations in LCA5 are a rare cause of childhood retinal dystrophy accounting for ?2% of disease in this cohort, and the majority of LCA5 mutations are likely null.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP977711.RA6DrdXk20O2p7GITbGmdxV_kXF3AEKQPqt17Ts0nxqi0130_provenance.