Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP615454.RAPvchXPxAqR_sWy78z0-TTV4k_Hh4fsKZI6ULaHUOBzM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP615454.RAPvchXPxAqR_sWy78z0-TTV4k_Hh4fsKZI6ULaHUOBzM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP615454.RAPvchXPxAqR_sWy78z0-TTV4k_Hh4fsKZI6ULaHUOBzM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP615454.RAPvchXPxAqR_sWy78z0-TTV4k_Hh4fsKZI6ULaHUOBzM130_provenance.
- NP615454.RAPvchXPxAqR_sWy78z0-TTV4k_Hh4fsKZI6ULaHUOBzM130_assertion description "[The causative gene for WS1 (WFS1) encoding wolframin maps to chromosome 4p16.1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP615454.RAPvchXPxAqR_sWy78z0-TTV4k_Hh4fsKZI6ULaHUOBzM130_provenance.
- NP615454.RAPvchXPxAqR_sWy78z0-TTV4k_Hh4fsKZI6ULaHUOBzM130_assertion evidence source_evidence_literature NP615454.RAPvchXPxAqR_sWy78z0-TTV4k_Hh4fsKZI6ULaHUOBzM130_provenance.
- NP615454.RAPvchXPxAqR_sWy78z0-TTV4k_Hh4fsKZI6ULaHUOBzM130_assertion SIO_000772 22790102 NP615454.RAPvchXPxAqR_sWy78z0-TTV4k_Hh4fsKZI6ULaHUOBzM130_provenance.
- NP615454.RAPvchXPxAqR_sWy78z0-TTV4k_Hh4fsKZI6ULaHUOBzM130_assertion wasDerivedFrom befree-20140225 NP615454.RAPvchXPxAqR_sWy78z0-TTV4k_Hh4fsKZI6ULaHUOBzM130_provenance.
- NP615454.RAPvchXPxAqR_sWy78z0-TTV4k_Hh4fsKZI6ULaHUOBzM130_assertion wasGeneratedBy ECO_0000203 NP615454.RAPvchXPxAqR_sWy78z0-TTV4k_Hh4fsKZI6ULaHUOBzM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP615454.RAPvchXPxAqR_sWy78z0-TTV4k_Hh4fsKZI6ULaHUOBzM130_provenance.