Matches in Nanopublications for { ?s ?p "[Mutations in KCNV2 have been proposed as the molecular basis for cone dystrophy with supernormal rod electroretinogram.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 2 of
2
with 100 items per page.
- NP745794.RAkffcrJegzLqV8iNwzUl4tffIXnafu6ooblTq7csU9do130_assertion description "[Mutations in KCNV2 have been proposed as the molecular basis for cone dystrophy with supernormal rod electroretinogram.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP745794.RAkffcrJegzLqV8iNwzUl4tffIXnafu6ooblTq7csU9do130_provenance.
- assertion description "[Mutations in KCNV2 have been proposed as the molecular basis for cone dystrophy with supernormal rod electroretinogram.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.