Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP441897.RAq2CPR5MFkwt2_DnDlZ1Z2AJh2kq8tdYdoUOY1PrRsPQ130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP441897.RAq2CPR5MFkwt2_DnDlZ1Z2AJh2kq8tdYdoUOY1PrRsPQ130_assertion type Assertion NP441897.RAq2CPR5MFkwt2_DnDlZ1Z2AJh2kq8tdYdoUOY1PrRsPQ130_head.
- NP441897.RAq2CPR5MFkwt2_DnDlZ1Z2AJh2kq8tdYdoUOY1PrRsPQ130_assertion description "[The patients analyzed included 52 with autosomal dominant retinitis pigmentosa, 36 with autosomal recessive retinitis pigmentosa, 3 with simplex retinitis pigmentosa, 12 with cone-rod dystrophy, 5 with rod-cone dystrophy, 3 with vitelliform macular dystrophy (Best's disease), 4 with macular dystrophy, 2 with cone dystrophy, 2 with fundus flavimaculatus, 2 with fundus albipunctatus, and 12 with retinitis pigmentosa with macular degeneration as well as 40 unrelated normal persons.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP441897.RAq2CPR5MFkwt2_DnDlZ1Z2AJh2kq8tdYdoUOY1PrRsPQ130_provenance.
- NP441897.RAq2CPR5MFkwt2_DnDlZ1Z2AJh2kq8tdYdoUOY1PrRsPQ130_assertion evidence source_evidence_literature NP441897.RAq2CPR5MFkwt2_DnDlZ1Z2AJh2kq8tdYdoUOY1PrRsPQ130_provenance.
- NP441897.RAq2CPR5MFkwt2_DnDlZ1Z2AJh2kq8tdYdoUOY1PrRsPQ130_assertion SIO_000772 9690896 NP441897.RAq2CPR5MFkwt2_DnDlZ1Z2AJh2kq8tdYdoUOY1PrRsPQ130_provenance.
- NP441897.RAq2CPR5MFkwt2_DnDlZ1Z2AJh2kq8tdYdoUOY1PrRsPQ130_assertion wasDerivedFrom befree-20150227 NP441897.RAq2CPR5MFkwt2_DnDlZ1Z2AJh2kq8tdYdoUOY1PrRsPQ130_provenance.
- NP441897.RAq2CPR5MFkwt2_DnDlZ1Z2AJh2kq8tdYdoUOY1PrRsPQ130_assertion wasGeneratedBy ECO_0000203 NP441897.RAq2CPR5MFkwt2_DnDlZ1Z2AJh2kq8tdYdoUOY1PrRsPQ130_provenance.