Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP867998.RABmXj0s9RHC78SciCwitRZz7c9dNH6GKEX3CNmzpn26U130_assertion> ?p ?o ?g. }
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- NP867998.RABmXj0s9RHC78SciCwitRZz7c9dNH6GKEX3CNmzpn26U130_assertion type Assertion NP867998.RABmXj0s9RHC78SciCwitRZz7c9dNH6GKEX3CNmzpn26U130_head.
- NP867998.RABmXj0s9RHC78SciCwitRZz7c9dNH6GKEX3CNmzpn26U130_assertion wasGeneratedBy ECO_0000203 NP867998.RABmXj0s9RHC78SciCwitRZz7c9dNH6GKEX3CNmzpn26U130_provenance.
- NP867998.RABmXj0s9RHC78SciCwitRZz7c9dNH6GKEX3CNmzpn26U130_assertion wasDerivedFrom befree-20140225 NP867998.RABmXj0s9RHC78SciCwitRZz7c9dNH6GKEX3CNmzpn26U130_provenance.
- NP867998.RABmXj0s9RHC78SciCwitRZz7c9dNH6GKEX3CNmzpn26U130_assertion SIO_000772 10521250 NP867998.RABmXj0s9RHC78SciCwitRZz7c9dNH6GKEX3CNmzpn26U130_provenance.
- NP867998.RABmXj0s9RHC78SciCwitRZz7c9dNH6GKEX3CNmzpn26U130_assertion evidence source_evidence_literature NP867998.RABmXj0s9RHC78SciCwitRZz7c9dNH6GKEX3CNmzpn26U130_provenance.
- NP867998.RABmXj0s9RHC78SciCwitRZz7c9dNH6GKEX3CNmzpn26U130_assertion description "[In order to determine the prevalence of rhodopsin alterations in southern French populations, we examined 52 unrelated patients/families with autosomal dominant RP (adRP=29), RP simplex (6), or unclassified RP (17).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP867998.RABmXj0s9RHC78SciCwitRZz7c9dNH6GKEX3CNmzpn26U130_provenance.