Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP282329.RAqvoJjEeiE0KzVlP1drPnsB0XwQN4uzfhpT667zh-8ts130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP282329.RAqvoJjEeiE0KzVlP1drPnsB0XwQN4uzfhpT667zh-8ts130_assertion type Assertion NP282329.RAqvoJjEeiE0KzVlP1drPnsB0XwQN4uzfhpT667zh-8ts130_head.
- NP282329.RAqvoJjEeiE0KzVlP1drPnsB0XwQN4uzfhpT667zh-8ts130_assertion description "[Mutations in PDE6A and the PDE6B genes lead to autosomal recessive (ar) forms of retinitis pigmentosa (RP) in human and to the homologous disease in dogs, designated generalised progressive retinal atrophy (gPRA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP282329.RAqvoJjEeiE0KzVlP1drPnsB0XwQN4uzfhpT667zh-8ts130_provenance.
- NP282329.RAqvoJjEeiE0KzVlP1drPnsB0XwQN4uzfhpT667zh-8ts130_assertion evidence source_evidence_literature NP282329.RAqvoJjEeiE0KzVlP1drPnsB0XwQN4uzfhpT667zh-8ts130_provenance.
- NP282329.RAqvoJjEeiE0KzVlP1drPnsB0XwQN4uzfhpT667zh-8ts130_assertion SIO_000772 10782214 NP282329.RAqvoJjEeiE0KzVlP1drPnsB0XwQN4uzfhpT667zh-8ts130_provenance.
- NP282329.RAqvoJjEeiE0KzVlP1drPnsB0XwQN4uzfhpT667zh-8ts130_assertion wasDerivedFrom befree-2016 NP282329.RAqvoJjEeiE0KzVlP1drPnsB0XwQN4uzfhpT667zh-8ts130_provenance.
- NP282329.RAqvoJjEeiE0KzVlP1drPnsB0XwQN4uzfhpT667zh-8ts130_assertion wasGeneratedBy ECO_0000203 NP282329.RAqvoJjEeiE0KzVlP1drPnsB0XwQN4uzfhpT667zh-8ts130_provenance.