Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP472222.RA8SRj4M672TIiLKVplxWt4a0ffUbP-YoaVJ3cIpuLP0w130_assertion> ?p ?o ?g. }
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- NP472222.RA8SRj4M672TIiLKVplxWt4a0ffUbP-YoaVJ3cIpuLP0w130_assertion type Assertion NP472222.RA8SRj4M672TIiLKVplxWt4a0ffUbP-YoaVJ3cIpuLP0w130_head.
- NP472222.RA8SRj4M672TIiLKVplxWt4a0ffUbP-YoaVJ3cIpuLP0w130_assertion description "[Missense mutations in NRL are associated with autosomal dominant retinitis pigmentosa; however, the phenotype associated with the loss of NRL function in humans has not been reported.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP472222.RA8SRj4M672TIiLKVplxWt4a0ffUbP-YoaVJ3cIpuLP0w130_provenance.
- NP472222.RA8SRj4M672TIiLKVplxWt4a0ffUbP-YoaVJ3cIpuLP0w130_assertion evidence source_evidence_literature NP472222.RA8SRj4M672TIiLKVplxWt4a0ffUbP-YoaVJ3cIpuLP0w130_provenance.
- NP472222.RA8SRj4M672TIiLKVplxWt4a0ffUbP-YoaVJ3cIpuLP0w130_assertion SIO_000772 15591106 NP472222.RA8SRj4M672TIiLKVplxWt4a0ffUbP-YoaVJ3cIpuLP0w130_provenance.
- NP472222.RA8SRj4M672TIiLKVplxWt4a0ffUbP-YoaVJ3cIpuLP0w130_assertion wasDerivedFrom befree-2016 NP472222.RA8SRj4M672TIiLKVplxWt4a0ffUbP-YoaVJ3cIpuLP0w130_provenance.
- NP472222.RA8SRj4M672TIiLKVplxWt4a0ffUbP-YoaVJ3cIpuLP0w130_assertion wasGeneratedBy ECO_0000203 NP472222.RA8SRj4M672TIiLKVplxWt4a0ffUbP-YoaVJ3cIpuLP0w130_provenance.