Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP907961.RAdIFa5t_lvbIJTuhWtzKunlYRdZT1zb1X-dDkaxThRxk130_assertion> ?p ?o ?g. }
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- NP907961.RAdIFa5t_lvbIJTuhWtzKunlYRdZT1zb1X-dDkaxThRxk130_assertion type Assertion NP907961.RAdIFa5t_lvbIJTuhWtzKunlYRdZT1zb1X-dDkaxThRxk130_head.
- NP907961.RAdIFa5t_lvbIJTuhWtzKunlYRdZT1zb1X-dDkaxThRxk130_assertion description "[To describe the clinical and genetic findings in two consanguineous families with Best vitelliform macular dystrophy (BVMD) and homozygous mutations in the bestrophin-1 (BEST1) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP907961.RAdIFa5t_lvbIJTuhWtzKunlYRdZT1zb1X-dDkaxThRxk130_provenance.
- NP907961.RAdIFa5t_lvbIJTuhWtzKunlYRdZT1zb1X-dDkaxThRxk130_assertion evidence source_evidence_literature NP907961.RAdIFa5t_lvbIJTuhWtzKunlYRdZT1zb1X-dDkaxThRxk130_provenance.
- NP907961.RAdIFa5t_lvbIJTuhWtzKunlYRdZT1zb1X-dDkaxThRxk130_assertion SIO_000772 21738390 NP907961.RAdIFa5t_lvbIJTuhWtzKunlYRdZT1zb1X-dDkaxThRxk130_provenance.
- NP907961.RAdIFa5t_lvbIJTuhWtzKunlYRdZT1zb1X-dDkaxThRxk130_assertion wasDerivedFrom befree-2016 NP907961.RAdIFa5t_lvbIJTuhWtzKunlYRdZT1zb1X-dDkaxThRxk130_provenance.
- NP907961.RAdIFa5t_lvbIJTuhWtzKunlYRdZT1zb1X-dDkaxThRxk130_assertion wasGeneratedBy ECO_0000203 NP907961.RAdIFa5t_lvbIJTuhWtzKunlYRdZT1zb1X-dDkaxThRxk130_provenance.