Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP783832.RAYvRw0uSI9q-jT6XQXxZmb1qd2jqmMpofFgtXyCYTPeI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP783832.RAYvRw0uSI9q-jT6XQXxZmb1qd2jqmMpofFgtXyCYTPeI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP783832.RAYvRw0uSI9q-jT6XQXxZmb1qd2jqmMpofFgtXyCYTPeI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP783832.RAYvRw0uSI9q-jT6XQXxZmb1qd2jqmMpofFgtXyCYTPeI130_provenance.
- NP783832.RAYvRw0uSI9q-jT6XQXxZmb1qd2jqmMpofFgtXyCYTPeI130_assertion description "[Two WNK isoforms, WNK1 and WNK4, have been identified as the disease genes for a rare monogenic hypertension syndrome (Gordon's syndrome or pseudohypoaldosteronism type 2 [PHA2]) implicating them in salt homeostasis by the kidney.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP783832.RAYvRw0uSI9q-jT6XQXxZmb1qd2jqmMpofFgtXyCYTPeI130_provenance.
- NP783832.RAYvRw0uSI9q-jT6XQXxZmb1qd2jqmMpofFgtXyCYTPeI130_assertion evidence source_evidence_literature NP783832.RAYvRw0uSI9q-jT6XQXxZmb1qd2jqmMpofFgtXyCYTPeI130_provenance.
- NP783832.RAYvRw0uSI9q-jT6XQXxZmb1qd2jqmMpofFgtXyCYTPeI130_assertion SIO_000772 15866321 NP783832.RAYvRw0uSI9q-jT6XQXxZmb1qd2jqmMpofFgtXyCYTPeI130_provenance.
- NP783832.RAYvRw0uSI9q-jT6XQXxZmb1qd2jqmMpofFgtXyCYTPeI130_assertion wasDerivedFrom befree-20150227 NP783832.RAYvRw0uSI9q-jT6XQXxZmb1qd2jqmMpofFgtXyCYTPeI130_provenance.
- NP783832.RAYvRw0uSI9q-jT6XQXxZmb1qd2jqmMpofFgtXyCYTPeI130_assertion wasGeneratedBy ECO_0000203 NP783832.RAYvRw0uSI9q-jT6XQXxZmb1qd2jqmMpofFgtXyCYTPeI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP783832.RAYvRw0uSI9q-jT6XQXxZmb1qd2jqmMpofFgtXyCYTPeI130_provenance.