Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP441559.RAKUSqQy2jtAmdNNS52k4Md9eBAkIC0sye2Qr_zGbRuW4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP441559.RAKUSqQy2jtAmdNNS52k4Md9eBAkIC0sye2Qr_zGbRuW4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP441559.RAKUSqQy2jtAmdNNS52k4Md9eBAkIC0sye2Qr_zGbRuW4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP441559.RAKUSqQy2jtAmdNNS52k4Md9eBAkIC0sye2Qr_zGbRuW4130_provenance.
- NP441559.RAKUSqQy2jtAmdNNS52k4Md9eBAkIC0sye2Qr_zGbRuW4130_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." NP441559.RAKUSqQy2jtAmdNNS52k4Md9eBAkIC0sye2Qr_zGbRuW4130_provenance.
- NP441559.RAKUSqQy2jtAmdNNS52k4Md9eBAkIC0sye2Qr_zGbRuW4130_assertion evidence source_evidence_literature NP441559.RAKUSqQy2jtAmdNNS52k4Md9eBAkIC0sye2Qr_zGbRuW4130_provenance.
- NP441559.RAKUSqQy2jtAmdNNS52k4Md9eBAkIC0sye2Qr_zGbRuW4130_assertion SIO_000772 15110905 NP441559.RAKUSqQy2jtAmdNNS52k4Md9eBAkIC0sye2Qr_zGbRuW4130_provenance.
- NP441559.RAKUSqQy2jtAmdNNS52k4Md9eBAkIC0sye2Qr_zGbRuW4130_assertion wasDerivedFrom befree-2016 NP441559.RAKUSqQy2jtAmdNNS52k4Md9eBAkIC0sye2Qr_zGbRuW4130_provenance.
- NP441559.RAKUSqQy2jtAmdNNS52k4Md9eBAkIC0sye2Qr_zGbRuW4130_assertion wasGeneratedBy ECO_0000203 NP441559.RAKUSqQy2jtAmdNNS52k4Md9eBAkIC0sye2Qr_zGbRuW4130_provenance.
- befree-2016 importedOn "2016-02-19" NP441559.RAKUSqQy2jtAmdNNS52k4Md9eBAkIC0sye2Qr_zGbRuW4130_provenance.