Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP920669.RA2Co4EhmYpEHQE09LwJ0JfIzji0uWerogChS7mJouZpM130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP920669.RA2Co4EhmYpEHQE09LwJ0JfIzji0uWerogChS7mJouZpM130_assertion type Assertion NP920669.RA2Co4EhmYpEHQE09LwJ0JfIzji0uWerogChS7mJouZpM130_head.
- NP920669.RA2Co4EhmYpEHQE09LwJ0JfIzji0uWerogChS7mJouZpM130_assertion description "[Large deletions of the KCNV2 gene are common in patients with cone dystrophy with supernormal rod response.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP920669.RA2Co4EhmYpEHQE09LwJ0JfIzji0uWerogChS7mJouZpM130_provenance.
- NP920669.RA2Co4EhmYpEHQE09LwJ0JfIzji0uWerogChS7mJouZpM130_assertion evidence source_evidence_literature NP920669.RA2Co4EhmYpEHQE09LwJ0JfIzji0uWerogChS7mJouZpM130_provenance.
- NP920669.RA2Co4EhmYpEHQE09LwJ0JfIzji0uWerogChS7mJouZpM130_assertion SIO_000772 21882291 NP920669.RA2Co4EhmYpEHQE09LwJ0JfIzji0uWerogChS7mJouZpM130_provenance.
- NP920669.RA2Co4EhmYpEHQE09LwJ0JfIzji0uWerogChS7mJouZpM130_assertion wasDerivedFrom befree-2016 NP920669.RA2Co4EhmYpEHQE09LwJ0JfIzji0uWerogChS7mJouZpM130_provenance.
- NP920669.RA2Co4EhmYpEHQE09LwJ0JfIzji0uWerogChS7mJouZpM130_assertion wasGeneratedBy ECO_0000203 NP920669.RA2Co4EhmYpEHQE09LwJ0JfIzji0uWerogChS7mJouZpM130_provenance.