Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP358608.RAsndbo7kCMlCIhR40B-UCNDENZJ0G8YfJWyAfnLAhMJ4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP358608.RAsndbo7kCMlCIhR40B-UCNDENZJ0G8YfJWyAfnLAhMJ4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP358608.RAsndbo7kCMlCIhR40B-UCNDENZJ0G8YfJWyAfnLAhMJ4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP358608.RAsndbo7kCMlCIhR40B-UCNDENZJ0G8YfJWyAfnLAhMJ4130_provenance.
- NP358608.RAsndbo7kCMlCIhR40B-UCNDENZJ0G8YfJWyAfnLAhMJ4130_assertion description "[The retinal degeneration in this patient is most likely to be secondary to a genetic disorder of autosomal or X-linked recessive inheritance rather than SCA6.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP358608.RAsndbo7kCMlCIhR40B-UCNDENZJ0G8YfJWyAfnLAhMJ4130_provenance.
- NP358608.RAsndbo7kCMlCIhR40B-UCNDENZJ0G8YfJWyAfnLAhMJ4130_assertion evidence source_evidence_literature NP358608.RAsndbo7kCMlCIhR40B-UCNDENZJ0G8YfJWyAfnLAhMJ4130_provenance.
- NP358608.RAsndbo7kCMlCIhR40B-UCNDENZJ0G8YfJWyAfnLAhMJ4130_assertion SIO_000772 12081723 NP358608.RAsndbo7kCMlCIhR40B-UCNDENZJ0G8YfJWyAfnLAhMJ4130_provenance.
- NP358608.RAsndbo7kCMlCIhR40B-UCNDENZJ0G8YfJWyAfnLAhMJ4130_assertion wasDerivedFrom befree-2016 NP358608.RAsndbo7kCMlCIhR40B-UCNDENZJ0G8YfJWyAfnLAhMJ4130_provenance.
- NP358608.RAsndbo7kCMlCIhR40B-UCNDENZJ0G8YfJWyAfnLAhMJ4130_assertion wasGeneratedBy ECO_0000203 NP358608.RAsndbo7kCMlCIhR40B-UCNDENZJ0G8YfJWyAfnLAhMJ4130_provenance.
- befree-2016 importedOn "2016-02-19" NP358608.RAsndbo7kCMlCIhR40B-UCNDENZJ0G8YfJWyAfnLAhMJ4130_provenance.