Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP668535.RAIvs8vgZXH3SjYDj8tydIRiYRYB9IxPFnnKcTvGDC22g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP668535.RAIvs8vgZXH3SjYDj8tydIRiYRYB9IxPFnnKcTvGDC22g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP668535.RAIvs8vgZXH3SjYDj8tydIRiYRYB9IxPFnnKcTvGDC22g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP668535.RAIvs8vgZXH3SjYDj8tydIRiYRYB9IxPFnnKcTvGDC22g130_provenance.
- NP668535.RAIvs8vgZXH3SjYDj8tydIRiYRYB9IxPFnnKcTvGDC22g130_assertion description "[A Swedish family with a mutation in the peripherin/RDS gene (Arg-172-Trp) associated with a progressive retinal degeneration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP668535.RAIvs8vgZXH3SjYDj8tydIRiYRYB9IxPFnnKcTvGDC22g130_provenance.
- NP668535.RAIvs8vgZXH3SjYDj8tydIRiYRYB9IxPFnnKcTvGDC22g130_assertion evidence source_evidence_literature NP668535.RAIvs8vgZXH3SjYDj8tydIRiYRYB9IxPFnnKcTvGDC22g130_provenance.
- NP668535.RAIvs8vgZXH3SjYDj8tydIRiYRYB9IxPFnnKcTvGDC22g130_assertion SIO_000772 9810570 NP668535.RAIvs8vgZXH3SjYDj8tydIRiYRYB9IxPFnnKcTvGDC22g130_provenance.
- NP668535.RAIvs8vgZXH3SjYDj8tydIRiYRYB9IxPFnnKcTvGDC22g130_assertion wasDerivedFrom befree-20150227 NP668535.RAIvs8vgZXH3SjYDj8tydIRiYRYB9IxPFnnKcTvGDC22g130_provenance.
- NP668535.RAIvs8vgZXH3SjYDj8tydIRiYRYB9IxPFnnKcTvGDC22g130_assertion wasGeneratedBy ECO_0000203 NP668535.RAIvs8vgZXH3SjYDj8tydIRiYRYB9IxPFnnKcTvGDC22g130_provenance.
- befree-20150227 importedOn "2015-02-27" NP668535.RAIvs8vgZXH3SjYDj8tydIRiYRYB9IxPFnnKcTvGDC22g130_provenance.