Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP916988.RAng1Du_-6nOlRDmXQxxchVE2oGNEhvK0xTVfOIW34U0c130_assertion> ?p ?o ?g. }
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- NP916988.RAng1Du_-6nOlRDmXQxxchVE2oGNEhvK0xTVfOIW34U0c130_assertion type Assertion NP916988.RAng1Du_-6nOlRDmXQxxchVE2oGNEhvK0xTVfOIW34U0c130_head.
- NP916988.RAng1Du_-6nOlRDmXQxxchVE2oGNEhvK0xTVfOIW34U0c130_assertion description "[Missense mutations in NRL are associated with autosomal dominant retinitis pigmentosa; however, the phenotype associated with the loss of NRL function in humans has not been reported.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP916988.RAng1Du_-6nOlRDmXQxxchVE2oGNEhvK0xTVfOIW34U0c130_provenance.
- NP916988.RAng1Du_-6nOlRDmXQxxchVE2oGNEhvK0xTVfOIW34U0c130_assertion evidence source_evidence_literature NP916988.RAng1Du_-6nOlRDmXQxxchVE2oGNEhvK0xTVfOIW34U0c130_provenance.
- NP916988.RAng1Du_-6nOlRDmXQxxchVE2oGNEhvK0xTVfOIW34U0c130_assertion SIO_000772 15591106 NP916988.RAng1Du_-6nOlRDmXQxxchVE2oGNEhvK0xTVfOIW34U0c130_provenance.
- NP916988.RAng1Du_-6nOlRDmXQxxchVE2oGNEhvK0xTVfOIW34U0c130_assertion wasDerivedFrom befree-20140225 NP916988.RAng1Du_-6nOlRDmXQxxchVE2oGNEhvK0xTVfOIW34U0c130_provenance.
- NP916988.RAng1Du_-6nOlRDmXQxxchVE2oGNEhvK0xTVfOIW34U0c130_assertion wasGeneratedBy ECO_0000203 NP916988.RAng1Du_-6nOlRDmXQxxchVE2oGNEhvK0xTVfOIW34U0c130_provenance.