Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP501179.RAfIklPU2eBcLaOUrakwBci01bOG4i4UXQ3sLwAUO8x-k130_assertion> ?p ?o ?g. }
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- NP501179.RAfIklPU2eBcLaOUrakwBci01bOG4i4UXQ3sLwAUO8x-k130_assertion type Assertion NP501179.RAfIklPU2eBcLaOUrakwBci01bOG4i4UXQ3sLwAUO8x-k130_head.
- NP501179.RAfIklPU2eBcLaOUrakwBci01bOG4i4UXQ3sLwAUO8x-k130_assertion description "[To investigate the retinal disease expression in USH2C, the subtype of Usher syndrome type 2 recently shown to be caused by mutation in the VLGR1 gene, and compare results with those from USH2A, a more common cause of Usher syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP501179.RAfIklPU2eBcLaOUrakwBci01bOG4i4UXQ3sLwAUO8x-k130_provenance.
- NP501179.RAfIklPU2eBcLaOUrakwBci01bOG4i4UXQ3sLwAUO8x-k130_assertion evidence source_evidence_literature NP501179.RAfIklPU2eBcLaOUrakwBci01bOG4i4UXQ3sLwAUO8x-k130_provenance.
- NP501179.RAfIklPU2eBcLaOUrakwBci01bOG4i4UXQ3sLwAUO8x-k130_assertion SIO_000772 15671307 NP501179.RAfIklPU2eBcLaOUrakwBci01bOG4i4UXQ3sLwAUO8x-k130_provenance.
- NP501179.RAfIklPU2eBcLaOUrakwBci01bOG4i4UXQ3sLwAUO8x-k130_assertion wasDerivedFrom befree-20140225 NP501179.RAfIklPU2eBcLaOUrakwBci01bOG4i4UXQ3sLwAUO8x-k130_provenance.
- NP501179.RAfIklPU2eBcLaOUrakwBci01bOG4i4UXQ3sLwAUO8x-k130_assertion wasGeneratedBy ECO_0000203 NP501179.RAfIklPU2eBcLaOUrakwBci01bOG4i4UXQ3sLwAUO8x-k130_provenance.