Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1407863.RA7_0-SAfsK4P16K0eEkIyM0ulQPBl8Sw0vsH4cRyUOi0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1407863.RA7_0-SAfsK4P16K0eEkIyM0ulQPBl8Sw0vsH4cRyUOi0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1407863.RA7_0-SAfsK4P16K0eEkIyM0ulQPBl8Sw0vsH4cRyUOi0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1407863.RA7_0-SAfsK4P16K0eEkIyM0ulQPBl8Sw0vsH4cRyUOi0130_provenance.
- NP1407863.RA7_0-SAfsK4P16K0eEkIyM0ulQPBl8Sw0vsH4cRyUOi0130_assertion description "[Earlier, the peripherin/RDS Arg-172-Trp mutation was associated primarily with a macular degeneration phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1407863.RA7_0-SAfsK4P16K0eEkIyM0ulQPBl8Sw0vsH4cRyUOi0130_provenance.
- NP1407863.RA7_0-SAfsK4P16K0eEkIyM0ulQPBl8Sw0vsH4cRyUOi0130_assertion evidence source_evidence_literature NP1407863.RA7_0-SAfsK4P16K0eEkIyM0ulQPBl8Sw0vsH4cRyUOi0130_provenance.
- NP1407863.RA7_0-SAfsK4P16K0eEkIyM0ulQPBl8Sw0vsH4cRyUOi0130_assertion SIO_000772 9810570 NP1407863.RA7_0-SAfsK4P16K0eEkIyM0ulQPBl8Sw0vsH4cRyUOi0130_provenance.
- NP1407863.RA7_0-SAfsK4P16K0eEkIyM0ulQPBl8Sw0vsH4cRyUOi0130_assertion wasDerivedFrom befree-2016 NP1407863.RA7_0-SAfsK4P16K0eEkIyM0ulQPBl8Sw0vsH4cRyUOi0130_provenance.
- NP1407863.RA7_0-SAfsK4P16K0eEkIyM0ulQPBl8Sw0vsH4cRyUOi0130_assertion wasGeneratedBy ECO_0000203 NP1407863.RA7_0-SAfsK4P16K0eEkIyM0ulQPBl8Sw0vsH4cRyUOi0130_provenance.
- befree-2016 importedOn "2016-02-19" NP1407863.RA7_0-SAfsK4P16K0eEkIyM0ulQPBl8Sw0vsH4cRyUOi0130_provenance.