Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP325891.RAhyHwoKUBTz5LqvYt14zgRRtcgB8iNmD_OSEDMRYjFvo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP325891.RAhyHwoKUBTz5LqvYt14zgRRtcgB8iNmD_OSEDMRYjFvo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP325891.RAhyHwoKUBTz5LqvYt14zgRRtcgB8iNmD_OSEDMRYjFvo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP325891.RAhyHwoKUBTz5LqvYt14zgRRtcgB8iNmD_OSEDMRYjFvo130_provenance.
- befree-2016 importedOn "2016-02-19" NP325891.RAhyHwoKUBTz5LqvYt14zgRRtcgB8iNmD_OSEDMRYjFvo130_provenance.
- NP325891.RAhyHwoKUBTz5LqvYt14zgRRtcgB8iNmD_OSEDMRYjFvo130_assertion wasGeneratedBy ECO_0000203 NP325891.RAhyHwoKUBTz5LqvYt14zgRRtcgB8iNmD_OSEDMRYjFvo130_provenance.
- NP325891.RAhyHwoKUBTz5LqvYt14zgRRtcgB8iNmD_OSEDMRYjFvo130_assertion wasDerivedFrom befree-2016 NP325891.RAhyHwoKUBTz5LqvYt14zgRRtcgB8iNmD_OSEDMRYjFvo130_provenance.
- NP325891.RAhyHwoKUBTz5LqvYt14zgRRtcgB8iNmD_OSEDMRYjFvo130_assertion SIO_000772 11485765 NP325891.RAhyHwoKUBTz5LqvYt14zgRRtcgB8iNmD_OSEDMRYjFvo130_provenance.
- NP325891.RAhyHwoKUBTz5LqvYt14zgRRtcgB8iNmD_OSEDMRYjFvo130_assertion evidence source_evidence_literature NP325891.RAhyHwoKUBTz5LqvYt14zgRRtcgB8iNmD_OSEDMRYjFvo130_provenance.
- NP325891.RAhyHwoKUBTz5LqvYt14zgRRtcgB8iNmD_OSEDMRYjFvo130_assertion description "[Peripherin/RDS gene mutation (Pro210Leu) and polymorphisms in Japanese patients with retinal dystrophies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP325891.RAhyHwoKUBTz5LqvYt14zgRRtcgB8iNmD_OSEDMRYjFvo130_provenance.