Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP775467.RAA2BUmy0NnRp2-0Q8abodCi-W-XYPkR0yV9syo1tdOtk130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP775467.RAA2BUmy0NnRp2-0Q8abodCi-W-XYPkR0yV9syo1tdOtk130_assertion type Assertion NP775467.RAA2BUmy0NnRp2-0Q8abodCi-W-XYPkR0yV9syo1tdOtk130_head.
- NP775467.RAA2BUmy0NnRp2-0Q8abodCi-W-XYPkR0yV9syo1tdOtk130_assertion wasGeneratedBy ECO_0000203 NP775467.RAA2BUmy0NnRp2-0Q8abodCi-W-XYPkR0yV9syo1tdOtk130_provenance.
- NP775467.RAA2BUmy0NnRp2-0Q8abodCi-W-XYPkR0yV9syo1tdOtk130_assertion wasDerivedFrom befree-20150227 NP775467.RAA2BUmy0NnRp2-0Q8abodCi-W-XYPkR0yV9syo1tdOtk130_provenance.
- NP775467.RAA2BUmy0NnRp2-0Q8abodCi-W-XYPkR0yV9syo1tdOtk130_assertion SIO_000772 24560797 NP775467.RAA2BUmy0NnRp2-0Q8abodCi-W-XYPkR0yV9syo1tdOtk130_provenance.
- NP775467.RAA2BUmy0NnRp2-0Q8abodCi-W-XYPkR0yV9syo1tdOtk130_assertion evidence source_evidence_literature NP775467.RAA2BUmy0NnRp2-0Q8abodCi-W-XYPkR0yV9syo1tdOtk130_provenance.
- NP775467.RAA2BUmy0NnRp2-0Q8abodCi-W-XYPkR0yV9syo1tdOtk130_assertion description "[Mutations in BEST1 cause five distinct retinal degenerative diseases, including adult vitelliform macular dystrophy (AVMD), autosomal recessive bestrophinopathy (ARB), autosomal dominant vitreoretinochoroidopathy (ADVIRC), and retinitis pigmentosa (RP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP775467.RAA2BUmy0NnRp2-0Q8abodCi-W-XYPkR0yV9syo1tdOtk130_provenance.