Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP650637.RAnGCY4uNkgq1AU48K41LA8njOcQzCQCzvOpg_6GbQeOA130_assertion> ?p ?o ?g. }
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- NP650637.RAnGCY4uNkgq1AU48K41LA8njOcQzCQCzvOpg_6GbQeOA130_assertion type Assertion NP650637.RAnGCY4uNkgq1AU48K41LA8njOcQzCQCzvOpg_6GbQeOA130_head.
- NP650637.RAnGCY4uNkgq1AU48K41LA8njOcQzCQCzvOpg_6GbQeOA130_assertion description "[Seventeen unrelated families with RP and an apparent X-linked pattern of disease inheritance were identified from the Swedish RP registry and screened for mutations in the RP2 and RPGR (for the RP3 disease) genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP650637.RAnGCY4uNkgq1AU48K41LA8njOcQzCQCzvOpg_6GbQeOA130_provenance.
- NP650637.RAnGCY4uNkgq1AU48K41LA8njOcQzCQCzvOpg_6GbQeOA130_assertion evidence source_evidence_literature NP650637.RAnGCY4uNkgq1AU48K41LA8njOcQzCQCzvOpg_6GbQeOA130_provenance.
- NP650637.RAnGCY4uNkgq1AU48K41LA8njOcQzCQCzvOpg_6GbQeOA130_assertion SIO_000772 14566651 NP650637.RAnGCY4uNkgq1AU48K41LA8njOcQzCQCzvOpg_6GbQeOA130_provenance.
- NP650637.RAnGCY4uNkgq1AU48K41LA8njOcQzCQCzvOpg_6GbQeOA130_assertion wasDerivedFrom befree-20140225 NP650637.RAnGCY4uNkgq1AU48K41LA8njOcQzCQCzvOpg_6GbQeOA130_provenance.
- NP650637.RAnGCY4uNkgq1AU48K41LA8njOcQzCQCzvOpg_6GbQeOA130_assertion wasGeneratedBy ECO_0000203 NP650637.RAnGCY4uNkgq1AU48K41LA8njOcQzCQCzvOpg_6GbQeOA130_provenance.