Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP613977.RAu5X0iFJhcCDKzds1alMQCY5RscfqzPxG2e5PhT63YXo130_assertion> ?p ?o ?g. }
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- NP613977.RAu5X0iFJhcCDKzds1alMQCY5RscfqzPxG2e5PhT63YXo130_assertion type Assertion NP613977.RAu5X0iFJhcCDKzds1alMQCY5RscfqzPxG2e5PhT63YXo130_head.
- NP613977.RAu5X0iFJhcCDKzds1alMQCY5RscfqzPxG2e5PhT63YXo130_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." NP613977.RAu5X0iFJhcCDKzds1alMQCY5RscfqzPxG2e5PhT63YXo130_provenance.
- NP613977.RAu5X0iFJhcCDKzds1alMQCY5RscfqzPxG2e5PhT63YXo130_assertion evidence source_evidence_literature NP613977.RAu5X0iFJhcCDKzds1alMQCY5RscfqzPxG2e5PhT63YXo130_provenance.
- NP613977.RAu5X0iFJhcCDKzds1alMQCY5RscfqzPxG2e5PhT63YXo130_assertion SIO_000772 10782214 NP613977.RAu5X0iFJhcCDKzds1alMQCY5RscfqzPxG2e5PhT63YXo130_provenance.
- NP613977.RAu5X0iFJhcCDKzds1alMQCY5RscfqzPxG2e5PhT63YXo130_assertion wasDerivedFrom befree-20150227 NP613977.RAu5X0iFJhcCDKzds1alMQCY5RscfqzPxG2e5PhT63YXo130_provenance.
- NP613977.RAu5X0iFJhcCDKzds1alMQCY5RscfqzPxG2e5PhT63YXo130_assertion wasGeneratedBy ECO_0000203 NP613977.RAu5X0iFJhcCDKzds1alMQCY5RscfqzPxG2e5PhT63YXo130_provenance.