Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP69289.RAnFZ9W6gUGuHTQRmwWuc9S4q6YHla019waeydml58nPQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP69289.RAnFZ9W6gUGuHTQRmwWuc9S4q6YHla019waeydml58nPQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP69289.RAnFZ9W6gUGuHTQRmwWuc9S4q6YHla019waeydml58nPQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP69289.RAnFZ9W6gUGuHTQRmwWuc9S4q6YHla019waeydml58nPQ130_provenance.
- NP69289.RAnFZ9W6gUGuHTQRmwWuc9S4q6YHla019waeydml58nPQ130_assertion description "[The DRB1*04-DQA1*03 haplotype is a marker of increased SO susceptibility and severity, as in Vogt-Koyanagi-Harada disease, which also has similar clinicopathological and HLA associations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP69289.RAnFZ9W6gUGuHTQRmwWuc9S4q6YHla019waeydml58nPQ130_provenance.
- NP69289.RAnFZ9W6gUGuHTQRmwWuc9S4q6YHla019waeydml58nPQ130_assertion evidence source_evidence_literature NP69289.RAnFZ9W6gUGuHTQRmwWuc9S4q6YHla019waeydml58nPQ130_provenance.
- NP69289.RAnFZ9W6gUGuHTQRmwWuc9S4q6YHla019waeydml58nPQ130_assertion SIO_000772 11222331 NP69289.RAnFZ9W6gUGuHTQRmwWuc9S4q6YHla019waeydml58nPQ130_provenance.
- NP69289.RAnFZ9W6gUGuHTQRmwWuc9S4q6YHla019waeydml58nPQ130_assertion wasDerivedFrom gad-20150221 NP69289.RAnFZ9W6gUGuHTQRmwWuc9S4q6YHla019waeydml58nPQ130_provenance.
- NP69289.RAnFZ9W6gUGuHTQRmwWuc9S4q6YHla019waeydml58nPQ130_assertion wasGeneratedBy ECO_0000203 NP69289.RAnFZ9W6gUGuHTQRmwWuc9S4q6YHla019waeydml58nPQ130_provenance.
- gad-20150221 importedOn "2015-02-21" NP69289.RAnFZ9W6gUGuHTQRmwWuc9S4q6YHla019waeydml58nPQ130_provenance.