Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP745794.RAkffcrJegzLqV8iNwzUl4tffIXnafu6ooblTq7csU9do130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP745794.RAkffcrJegzLqV8iNwzUl4tffIXnafu6ooblTq7csU9do130_assertion type Assertion NP745794.RAkffcrJegzLqV8iNwzUl4tffIXnafu6ooblTq7csU9do130_head.
- 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.
- NP745794.RAkffcrJegzLqV8iNwzUl4tffIXnafu6ooblTq7csU9do130_assertion evidence source_evidence_literature NP745794.RAkffcrJegzLqV8iNwzUl4tffIXnafu6ooblTq7csU9do130_provenance.
- NP745794.RAkffcrJegzLqV8iNwzUl4tffIXnafu6ooblTq7csU9do130_assertion SIO_000772 23115240 NP745794.RAkffcrJegzLqV8iNwzUl4tffIXnafu6ooblTq7csU9do130_provenance.
- NP745794.RAkffcrJegzLqV8iNwzUl4tffIXnafu6ooblTq7csU9do130_assertion wasDerivedFrom befree-20140225 NP745794.RAkffcrJegzLqV8iNwzUl4tffIXnafu6ooblTq7csU9do130_provenance.
- NP745794.RAkffcrJegzLqV8iNwzUl4tffIXnafu6ooblTq7csU9do130_assertion wasGeneratedBy ECO_0000203 NP745794.RAkffcrJegzLqV8iNwzUl4tffIXnafu6ooblTq7csU9do130_provenance.