Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP330109.RAKgVGnkGH5r9JtwKLhvJFVQsrvv3C2xyWRJA6-WYc0yA130_assertion> ?p ?o ?g. }
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- NP330109.RAKgVGnkGH5r9JtwKLhvJFVQsrvv3C2xyWRJA6-WYc0yA130_assertion type Assertion NP330109.RAKgVGnkGH5r9JtwKLhvJFVQsrvv3C2xyWRJA6-WYc0yA130_head.
- NP330109.RAKgVGnkGH5r9JtwKLhvJFVQsrvv3C2xyWRJA6-WYc0yA130_assertion description "[For example, mutations in the ABCR gene, (recently identified in cones as well) which codes for retinal rod-specific ABCR protein is responsible for Stargardt macular dystrophy/fundus flavimaculatus, an autosomal recessive macular dystrophy with juvenile onset, which accounts for 7% of human retinal degenerative diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP330109.RAKgVGnkGH5r9JtwKLhvJFVQsrvv3C2xyWRJA6-WYc0yA130_provenance.
- NP330109.RAKgVGnkGH5r9JtwKLhvJFVQsrvv3C2xyWRJA6-WYc0yA130_assertion evidence source_evidence_literature NP330109.RAKgVGnkGH5r9JtwKLhvJFVQsrvv3C2xyWRJA6-WYc0yA130_provenance.
- NP330109.RAKgVGnkGH5r9JtwKLhvJFVQsrvv3C2xyWRJA6-WYc0yA130_assertion SIO_000772 11556484 NP330109.RAKgVGnkGH5r9JtwKLhvJFVQsrvv3C2xyWRJA6-WYc0yA130_provenance.
- NP330109.RAKgVGnkGH5r9JtwKLhvJFVQsrvv3C2xyWRJA6-WYc0yA130_assertion wasDerivedFrom befree-2016 NP330109.RAKgVGnkGH5r9JtwKLhvJFVQsrvv3C2xyWRJA6-WYc0yA130_provenance.
- NP330109.RAKgVGnkGH5r9JtwKLhvJFVQsrvv3C2xyWRJA6-WYc0yA130_assertion wasGeneratedBy ECO_0000203 NP330109.RAKgVGnkGH5r9JtwKLhvJFVQsrvv3C2xyWRJA6-WYc0yA130_provenance.