Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1407859.RAUTm22dTRQG5RBo6FLB6gHjp41ooz1yRPgKmT-Dz2svc130_assertion> ?p ?o ?g. }
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- NP1407859.RAUTm22dTRQG5RBo6FLB6gHjp41ooz1yRPgKmT-Dz2svc130_assertion type Assertion NP1407859.RAUTm22dTRQG5RBo6FLB6gHjp41ooz1yRPgKmT-Dz2svc130_head.
- NP1407859.RAUTm22dTRQG5RBo6FLB6gHjp41ooz1yRPgKmT-Dz2svc130_assertion description "[Mutations in the retina-specific ATP-binding cassette transporter gene (ABCR) cause recessive Stargardt's disease (STGD) and fundus flavimaculatus (FFM), and were also found in 16% of patients with AMD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1407859.RAUTm22dTRQG5RBo6FLB6gHjp41ooz1yRPgKmT-Dz2svc130_provenance.
- NP1407859.RAUTm22dTRQG5RBo6FLB6gHjp41ooz1yRPgKmT-Dz2svc130_assertion evidence source_evidence_literature NP1407859.RAUTm22dTRQG5RBo6FLB6gHjp41ooz1yRPgKmT-Dz2svc130_provenance.
- NP1407859.RAUTm22dTRQG5RBo6FLB6gHjp41ooz1yRPgKmT-Dz2svc130_assertion SIO_000772 9810566 NP1407859.RAUTm22dTRQG5RBo6FLB6gHjp41ooz1yRPgKmT-Dz2svc130_provenance.
- NP1407859.RAUTm22dTRQG5RBo6FLB6gHjp41ooz1yRPgKmT-Dz2svc130_assertion wasDerivedFrom befree-2016 NP1407859.RAUTm22dTRQG5RBo6FLB6gHjp41ooz1yRPgKmT-Dz2svc130_provenance.
- NP1407859.RAUTm22dTRQG5RBo6FLB6gHjp41ooz1yRPgKmT-Dz2svc130_assertion wasGeneratedBy ECO_0000203 NP1407859.RAUTm22dTRQG5RBo6FLB6gHjp41ooz1yRPgKmT-Dz2svc130_provenance.