Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP602266.RAwGZA_IpCoccV__woxn1MuiGMGjroWGN-5yOB7RVc03k130_assertion> ?p ?o ?g. }
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- NP602266.RAwGZA_IpCoccV__woxn1MuiGMGjroWGN-5yOB7RVc03k130_assertion type Assertion NP602266.RAwGZA_IpCoccV__woxn1MuiGMGjroWGN-5yOB7RVc03k130_head.
- NP602266.RAwGZA_IpCoccV__woxn1MuiGMGjroWGN-5yOB7RVc03k130_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." NP602266.RAwGZA_IpCoccV__woxn1MuiGMGjroWGN-5yOB7RVc03k130_provenance.
- NP602266.RAwGZA_IpCoccV__woxn1MuiGMGjroWGN-5yOB7RVc03k130_assertion evidence source_evidence_literature NP602266.RAwGZA_IpCoccV__woxn1MuiGMGjroWGN-5yOB7RVc03k130_provenance.
- NP602266.RAwGZA_IpCoccV__woxn1MuiGMGjroWGN-5yOB7RVc03k130_assertion SIO_000772 10782214 NP602266.RAwGZA_IpCoccV__woxn1MuiGMGjroWGN-5yOB7RVc03k130_provenance.
- NP602266.RAwGZA_IpCoccV__woxn1MuiGMGjroWGN-5yOB7RVc03k130_assertion wasDerivedFrom befree-20140225 NP602266.RAwGZA_IpCoccV__woxn1MuiGMGjroWGN-5yOB7RVc03k130_provenance.
- NP602266.RAwGZA_IpCoccV__woxn1MuiGMGjroWGN-5yOB7RVc03k130_assertion wasGeneratedBy ECO_0000203 NP602266.RAwGZA_IpCoccV__woxn1MuiGMGjroWGN-5yOB7RVc03k130_provenance.