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- NP525720.RAafy2h-z3cHwjFyiCy3xO6l0tk20N_pFYNcY3pXetcrA130_assertion type Assertion NP525720.RAafy2h-z3cHwjFyiCy3xO6l0tk20N_pFYNcY3pXetcrA130_head.
- NP525720.RAafy2h-z3cHwjFyiCy3xO6l0tk20N_pFYNcY3pXetcrA130_assertion description "[We describe a distinct retinal disorder, autosomal-recessive bestrophinopathy (ARB), that is consequent upon biallelic mutation in BEST1 and is associated with central visual loss, a characteristic retinopathy, an absent electro-oculogram light rise, and a reduced electroretinogram.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP525720.RAafy2h-z3cHwjFyiCy3xO6l0tk20N_pFYNcY3pXetcrA130_provenance.
- NP525720.RAafy2h-z3cHwjFyiCy3xO6l0tk20N_pFYNcY3pXetcrA130_assertion evidence source_evidence_literature NP525720.RAafy2h-z3cHwjFyiCy3xO6l0tk20N_pFYNcY3pXetcrA130_provenance.
- NP525720.RAafy2h-z3cHwjFyiCy3xO6l0tk20N_pFYNcY3pXetcrA130_assertion SIO_000772 18179881 NP525720.RAafy2h-z3cHwjFyiCy3xO6l0tk20N_pFYNcY3pXetcrA130_provenance.
- NP525720.RAafy2h-z3cHwjFyiCy3xO6l0tk20N_pFYNcY3pXetcrA130_assertion wasDerivedFrom befree-20140225 NP525720.RAafy2h-z3cHwjFyiCy3xO6l0tk20N_pFYNcY3pXetcrA130_provenance.
- NP525720.RAafy2h-z3cHwjFyiCy3xO6l0tk20N_pFYNcY3pXetcrA130_assertion wasGeneratedBy ECO_0000203 NP525720.RAafy2h-z3cHwjFyiCy3xO6l0tk20N_pFYNcY3pXetcrA130_provenance.