Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP315493.RAee_DF45ryG0USR0Y5Gi9kGxIWvKJwfWmeh3H69WQcwQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP315493.RAee_DF45ryG0USR0Y5Gi9kGxIWvKJwfWmeh3H69WQcwQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP315493.RAee_DF45ryG0USR0Y5Gi9kGxIWvKJwfWmeh3H69WQcwQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP315493.RAee_DF45ryG0USR0Y5Gi9kGxIWvKJwfWmeh3H69WQcwQ130_provenance.
- NP315493.RAee_DF45ryG0USR0Y5Gi9kGxIWvKJwfWmeh3H69WQcwQ130_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." NP315493.RAee_DF45ryG0USR0Y5Gi9kGxIWvKJwfWmeh3H69WQcwQ130_provenance.
- NP315493.RAee_DF45ryG0USR0Y5Gi9kGxIWvKJwfWmeh3H69WQcwQ130_assertion evidence source_evidence_literature NP315493.RAee_DF45ryG0USR0Y5Gi9kGxIWvKJwfWmeh3H69WQcwQ130_provenance.
- NP315493.RAee_DF45ryG0USR0Y5Gi9kGxIWvKJwfWmeh3H69WQcwQ130_assertion SIO_000772 20810575 NP315493.RAee_DF45ryG0USR0Y5Gi9kGxIWvKJwfWmeh3H69WQcwQ130_provenance.
- NP315493.RAee_DF45ryG0USR0Y5Gi9kGxIWvKJwfWmeh3H69WQcwQ130_assertion wasDerivedFrom befree-20150227 NP315493.RAee_DF45ryG0USR0Y5Gi9kGxIWvKJwfWmeh3H69WQcwQ130_provenance.
- NP315493.RAee_DF45ryG0USR0Y5Gi9kGxIWvKJwfWmeh3H69WQcwQ130_assertion wasGeneratedBy ECO_0000203 NP315493.RAee_DF45ryG0USR0Y5Gi9kGxIWvKJwfWmeh3H69WQcwQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP315493.RAee_DF45ryG0USR0Y5Gi9kGxIWvKJwfWmeh3H69WQcwQ130_provenance.