Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP525593.RAY6Smic6q8OuXepSWyowz3sGeWSxQZHKD0-vSlZejkZE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP525593.RAY6Smic6q8OuXepSWyowz3sGeWSxQZHKD0-vSlZejkZE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP525593.RAY6Smic6q8OuXepSWyowz3sGeWSxQZHKD0-vSlZejkZE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP525593.RAY6Smic6q8OuXepSWyowz3sGeWSxQZHKD0-vSlZejkZE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP525593.RAY6Smic6q8OuXepSWyowz3sGeWSxQZHKD0-vSlZejkZE130_provenance.
- NP525593.RAY6Smic6q8OuXepSWyowz3sGeWSxQZHKD0-vSlZejkZE130_assertion wasGeneratedBy ECO_0000203 NP525593.RAY6Smic6q8OuXepSWyowz3sGeWSxQZHKD0-vSlZejkZE130_provenance.
- NP525593.RAY6Smic6q8OuXepSWyowz3sGeWSxQZHKD0-vSlZejkZE130_assertion wasDerivedFrom befree-20150227 NP525593.RAY6Smic6q8OuXepSWyowz3sGeWSxQZHKD0-vSlZejkZE130_provenance.
- NP525593.RAY6Smic6q8OuXepSWyowz3sGeWSxQZHKD0-vSlZejkZE130_assertion SIO_000772 16619012 NP525593.RAY6Smic6q8OuXepSWyowz3sGeWSxQZHKD0-vSlZejkZE130_provenance.
- NP525593.RAY6Smic6q8OuXepSWyowz3sGeWSxQZHKD0-vSlZejkZE130_assertion evidence source_evidence_literature NP525593.RAY6Smic6q8OuXepSWyowz3sGeWSxQZHKD0-vSlZejkZE130_provenance.
- NP525593.RAY6Smic6q8OuXepSWyowz3sGeWSxQZHKD0-vSlZejkZE130_assertion description "[These results are consistent with the previous hypothesis that progressive piebaldism might result from digenic inheritance, of the KIT(V620A) mutation that causes piebaldism and a second, unknown locus that causes progressive depigmentation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP525593.RAY6Smic6q8OuXepSWyowz3sGeWSxQZHKD0-vSlZejkZE130_provenance.