Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP658377.RAAr4yNMViLUR2YPOsFWKl6otFXJT9oVAo93i5AxwXE-c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP658377.RAAr4yNMViLUR2YPOsFWKl6otFXJT9oVAo93i5AxwXE-c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP658377.RAAr4yNMViLUR2YPOsFWKl6otFXJT9oVAo93i5AxwXE-c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP658377.RAAr4yNMViLUR2YPOsFWKl6otFXJT9oVAo93i5AxwXE-c130_provenance.
- NP658377.RAAr4yNMViLUR2YPOsFWKl6otFXJT9oVAo93i5AxwXE-c130_assertion description "[We have recently demonstrated that two inherited skin diseases, Vohwinkel's syndrome (VS) and progressive symmetric erythrokeratoderma (PSEK) may result from mutations in the gene encoding loricrin, a major constituent of the CE.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP658377.RAAr4yNMViLUR2YPOsFWKl6otFXJT9oVAo93i5AxwXE-c130_provenance.
- NP658377.RAAr4yNMViLUR2YPOsFWKl6otFXJT9oVAo93i5AxwXE-c130_assertion evidence source_evidence_literature NP658377.RAAr4yNMViLUR2YPOsFWKl6otFXJT9oVAo93i5AxwXE-c130_provenance.
- NP658377.RAAr4yNMViLUR2YPOsFWKl6otFXJT9oVAo93i5AxwXE-c130_assertion SIO_000772 9690138 NP658377.RAAr4yNMViLUR2YPOsFWKl6otFXJT9oVAo93i5AxwXE-c130_provenance.
- NP658377.RAAr4yNMViLUR2YPOsFWKl6otFXJT9oVAo93i5AxwXE-c130_assertion wasDerivedFrom befree-20140225 NP658377.RAAr4yNMViLUR2YPOsFWKl6otFXJT9oVAo93i5AxwXE-c130_provenance.
- NP658377.RAAr4yNMViLUR2YPOsFWKl6otFXJT9oVAo93i5AxwXE-c130_assertion wasGeneratedBy ECO_0000203 NP658377.RAAr4yNMViLUR2YPOsFWKl6otFXJT9oVAo93i5AxwXE-c130_provenance.
- befree-20140225 importedOn "2014-02-25" NP658377.RAAr4yNMViLUR2YPOsFWKl6otFXJT9oVAo93i5AxwXE-c130_provenance.