Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP941538.RAssjah_pnOSxFOAqu5rg7g6lFqnk42LPLESwJQ4UIvdU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP941538.RAssjah_pnOSxFOAqu5rg7g6lFqnk42LPLESwJQ4UIvdU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP941538.RAssjah_pnOSxFOAqu5rg7g6lFqnk42LPLESwJQ4UIvdU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP941538.RAssjah_pnOSxFOAqu5rg7g6lFqnk42LPLESwJQ4UIvdU130_provenance.
- NP941538.RAssjah_pnOSxFOAqu5rg7g6lFqnk42LPLESwJQ4UIvdU130_assertion description "[Although substantial contribution of three novel missense mutations in exons 7 and 17 of WNK4 to the genetics of hypertension or renal failure is still unclear, these mutations in the WNK4 gene identified in Japanese hypertensives but not in a general population may contribute to hypertension and progression of hypertensive complications to some extent.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP941538.RAssjah_pnOSxFOAqu5rg7g6lFqnk42LPLESwJQ4UIvdU130_provenance.
- NP941538.RAssjah_pnOSxFOAqu5rg7g6lFqnk42LPLESwJQ4UIvdU130_assertion evidence source_evidence_literature NP941538.RAssjah_pnOSxFOAqu5rg7g6lFqnk42LPLESwJQ4UIvdU130_provenance.
- NP941538.RAssjah_pnOSxFOAqu5rg7g6lFqnk42LPLESwJQ4UIvdU130_assertion SIO_000772 15110905 NP941538.RAssjah_pnOSxFOAqu5rg7g6lFqnk42LPLESwJQ4UIvdU130_provenance.
- NP941538.RAssjah_pnOSxFOAqu5rg7g6lFqnk42LPLESwJQ4UIvdU130_assertion wasDerivedFrom befree-20150227 NP941538.RAssjah_pnOSxFOAqu5rg7g6lFqnk42LPLESwJQ4UIvdU130_provenance.
- NP941538.RAssjah_pnOSxFOAqu5rg7g6lFqnk42LPLESwJQ4UIvdU130_assertion wasGeneratedBy ECO_0000203 NP941538.RAssjah_pnOSxFOAqu5rg7g6lFqnk42LPLESwJQ4UIvdU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP941538.RAssjah_pnOSxFOAqu5rg7g6lFqnk42LPLESwJQ4UIvdU130_provenance.