Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP650637.RAnGCY4uNkgq1AU48K41LA8njOcQzCQCzvOpg_6GbQeOA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP650637.RAnGCY4uNkgq1AU48K41LA8njOcQzCQCzvOpg_6GbQeOA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP650637.RAnGCY4uNkgq1AU48K41LA8njOcQzCQCzvOpg_6GbQeOA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP650637.RAnGCY4uNkgq1AU48K41LA8njOcQzCQCzvOpg_6GbQeOA130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP650637.RAnGCY4uNkgq1AU48K41LA8njOcQzCQCzvOpg_6GbQeOA130_provenance.