Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1009190.RAR50m2GO7_8XHSj-Q6VPLvRmNr-YSziaNQhErRQg6eto130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1009190.RAR50m2GO7_8XHSj-Q6VPLvRmNr-YSziaNQhErRQg6eto130_assertion type Assertion NP1009190.RAR50m2GO7_8XHSj-Q6VPLvRmNr-YSziaNQhErRQg6eto130_head.
- NP1009190.RAR50m2GO7_8XHSj-Q6VPLvRmNr-YSziaNQhErRQg6eto130_assertion wasGeneratedBy ECO_0000203 NP1009190.RAR50m2GO7_8XHSj-Q6VPLvRmNr-YSziaNQhErRQg6eto130_provenance.
- NP1009190.RAR50m2GO7_8XHSj-Q6VPLvRmNr-YSziaNQhErRQg6eto130_assertion wasDerivedFrom befree-20150227 NP1009190.RAR50m2GO7_8XHSj-Q6VPLvRmNr-YSziaNQhErRQg6eto130_provenance.
- NP1009190.RAR50m2GO7_8XHSj-Q6VPLvRmNr-YSziaNQhErRQg6eto130_assertion SIO_000772 16384941 NP1009190.RAR50m2GO7_8XHSj-Q6VPLvRmNr-YSziaNQhErRQg6eto130_provenance.
- NP1009190.RAR50m2GO7_8XHSj-Q6VPLvRmNr-YSziaNQhErRQg6eto130_assertion evidence source_evidence_literature NP1009190.RAR50m2GO7_8XHSj-Q6VPLvRmNr-YSziaNQhErRQg6eto130_provenance.
- NP1009190.RAR50m2GO7_8XHSj-Q6VPLvRmNr-YSziaNQhErRQg6eto130_assertion description "[The coding sequence and flanking intron/exon junctions of IMPDH1 were analyzed in 203 patients with autosomal dominant RP (adRP), 55 patients with autosomal recessive RP (arRP), 7 patients with isolated RP, 17 patients with macular degeneration (MD), and 24 patients with Leber congenital amaurosis (LCA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1009190.RAR50m2GO7_8XHSj-Q6VPLvRmNr-YSziaNQhErRQg6eto130_provenance.