Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP718590.RAQUCXpnpnGVqjNbEZ5041msHI9mZb0MwPyPY_Drrp53U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP718590.RAQUCXpnpnGVqjNbEZ5041msHI9mZb0MwPyPY_Drrp53U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP718590.RAQUCXpnpnGVqjNbEZ5041msHI9mZb0MwPyPY_Drrp53U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP718590.RAQUCXpnpnGVqjNbEZ5041msHI9mZb0MwPyPY_Drrp53U130_provenance.
- NP718590.RAQUCXpnpnGVqjNbEZ5041msHI9mZb0MwPyPY_Drrp53U130_assertion description "[Expanding the clinical phenotype associated with ELOVL4 mutation: study of a large French-Canadian family with autosomal dominant spinocerebellar ataxia and erythrokeratodermia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP718590.RAQUCXpnpnGVqjNbEZ5041msHI9mZb0MwPyPY_Drrp53U130_provenance.
- NP718590.RAQUCXpnpnGVqjNbEZ5041msHI9mZb0MwPyPY_Drrp53U130_assertion evidence source_evidence_literature NP718590.RAQUCXpnpnGVqjNbEZ5041msHI9mZb0MwPyPY_Drrp53U130_provenance.
- NP718590.RAQUCXpnpnGVqjNbEZ5041msHI9mZb0MwPyPY_Drrp53U130_assertion SIO_000772 24566826 NP718590.RAQUCXpnpnGVqjNbEZ5041msHI9mZb0MwPyPY_Drrp53U130_provenance.
- NP718590.RAQUCXpnpnGVqjNbEZ5041msHI9mZb0MwPyPY_Drrp53U130_assertion wasDerivedFrom befree-20150227 NP718590.RAQUCXpnpnGVqjNbEZ5041msHI9mZb0MwPyPY_Drrp53U130_provenance.
- NP718590.RAQUCXpnpnGVqjNbEZ5041msHI9mZb0MwPyPY_Drrp53U130_assertion wasGeneratedBy ECO_0000203 NP718590.RAQUCXpnpnGVqjNbEZ5041msHI9mZb0MwPyPY_Drrp53U130_provenance.
- befree-20150227 importedOn "2015-02-27" NP718590.RAQUCXpnpnGVqjNbEZ5041msHI9mZb0MwPyPY_Drrp53U130_provenance.