Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP836487.RATU1N8lrnauFIHiiNhZHtvwlVKfzuolrb7u8bAxY4c2k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP836487.RATU1N8lrnauFIHiiNhZHtvwlVKfzuolrb7u8bAxY4c2k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP836487.RATU1N8lrnauFIHiiNhZHtvwlVKfzuolrb7u8bAxY4c2k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP836487.RATU1N8lrnauFIHiiNhZHtvwlVKfzuolrb7u8bAxY4c2k130_provenance.
- NP836487.RATU1N8lrnauFIHiiNhZHtvwlVKfzuolrb7u8bAxY4c2k130_assertion description "[This study revealed the following characteristics of these disorders: 1) subjects with CLCNKB mutations showed one or more biochemical features of Gitelman syndrome (including hypomagnesemia, hypocalciuria, and fractional chloride excretion insensitivity to thiazide administration); and 2) subjects with KCNJ1 mutations appeared to show normal fractional chloride excretion sensitivity to furosemide and thiazide administration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP836487.RATU1N8lrnauFIHiiNhZHtvwlVKfzuolrb7u8bAxY4c2k130_provenance.
- NP836487.RATU1N8lrnauFIHiiNhZHtvwlVKfzuolrb7u8bAxY4c2k130_assertion evidence source_evidence_literature NP836487.RATU1N8lrnauFIHiiNhZHtvwlVKfzuolrb7u8bAxY4c2k130_provenance.
- NP836487.RATU1N8lrnauFIHiiNhZHtvwlVKfzuolrb7u8bAxY4c2k130_assertion SIO_000772 20810575 NP836487.RATU1N8lrnauFIHiiNhZHtvwlVKfzuolrb7u8bAxY4c2k130_provenance.
- NP836487.RATU1N8lrnauFIHiiNhZHtvwlVKfzuolrb7u8bAxY4c2k130_assertion wasDerivedFrom befree-2016 NP836487.RATU1N8lrnauFIHiiNhZHtvwlVKfzuolrb7u8bAxY4c2k130_provenance.
- NP836487.RATU1N8lrnauFIHiiNhZHtvwlVKfzuolrb7u8bAxY4c2k130_assertion wasGeneratedBy ECO_0000203 NP836487.RATU1N8lrnauFIHiiNhZHtvwlVKfzuolrb7u8bAxY4c2k130_provenance.
- befree-2016 importedOn "2016-02-19" NP836487.RATU1N8lrnauFIHiiNhZHtvwlVKfzuolrb7u8bAxY4c2k130_provenance.