Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP577766.RAftUpRNTfWOZEhcVFRNgSUy6z-eP4xVAas83wXE1vrBs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP577766.RAftUpRNTfWOZEhcVFRNgSUy6z-eP4xVAas83wXE1vrBs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP577766.RAftUpRNTfWOZEhcVFRNgSUy6z-eP4xVAas83wXE1vrBs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP577766.RAftUpRNTfWOZEhcVFRNgSUy6z-eP4xVAas83wXE1vrBs130_provenance.
- NP577766.RAftUpRNTfWOZEhcVFRNgSUy6z-eP4xVAas83wXE1vrBs130_assertion description "[Mutations in the peripherin/retinal degeneration slow (RDS) gene have been identified in patients with retinitis pigmentosa and pattern macular dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP577766.RAftUpRNTfWOZEhcVFRNgSUy6z-eP4xVAas83wXE1vrBs130_provenance.
- NP577766.RAftUpRNTfWOZEhcVFRNgSUy6z-eP4xVAas83wXE1vrBs130_assertion evidence source_evidence_literature NP577766.RAftUpRNTfWOZEhcVFRNgSUy6z-eP4xVAas83wXE1vrBs130_provenance.
- NP577766.RAftUpRNTfWOZEhcVFRNgSUy6z-eP4xVAas83wXE1vrBs130_assertion SIO_000772 7862413 NP577766.RAftUpRNTfWOZEhcVFRNgSUy6z-eP4xVAas83wXE1vrBs130_provenance.
- NP577766.RAftUpRNTfWOZEhcVFRNgSUy6z-eP4xVAas83wXE1vrBs130_assertion wasDerivedFrom befree-20140225 NP577766.RAftUpRNTfWOZEhcVFRNgSUy6z-eP4xVAas83wXE1vrBs130_provenance.
- NP577766.RAftUpRNTfWOZEhcVFRNgSUy6z-eP4xVAas83wXE1vrBs130_assertion wasGeneratedBy ECO_0000203 NP577766.RAftUpRNTfWOZEhcVFRNgSUy6z-eP4xVAas83wXE1vrBs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP577766.RAftUpRNTfWOZEhcVFRNgSUy6z-eP4xVAas83wXE1vrBs130_provenance.