Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP441561.RAZ0pjqFoj5txlgQ6FnSSOn8_8uEQFbU6hzfaiFOLHE4A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP441561.RAZ0pjqFoj5txlgQ6FnSSOn8_8uEQFbU6hzfaiFOLHE4A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP441561.RAZ0pjqFoj5txlgQ6FnSSOn8_8uEQFbU6hzfaiFOLHE4A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP441561.RAZ0pjqFoj5txlgQ6FnSSOn8_8uEQFbU6hzfaiFOLHE4A130_provenance.
- NP441561.RAZ0pjqFoj5txlgQ6FnSSOn8_8uEQFbU6hzfaiFOLHE4A130_assertion description "[We screened 956 Japanese patients with hypertension or renal failure for mutations in exons 7 and 17 in the WNK4 gene where the mutations were identified in patients with PHAII.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP441561.RAZ0pjqFoj5txlgQ6FnSSOn8_8uEQFbU6hzfaiFOLHE4A130_provenance.
- NP441561.RAZ0pjqFoj5txlgQ6FnSSOn8_8uEQFbU6hzfaiFOLHE4A130_assertion evidence source_evidence_literature NP441561.RAZ0pjqFoj5txlgQ6FnSSOn8_8uEQFbU6hzfaiFOLHE4A130_provenance.
- NP441561.RAZ0pjqFoj5txlgQ6FnSSOn8_8uEQFbU6hzfaiFOLHE4A130_assertion SIO_000772 15110905 NP441561.RAZ0pjqFoj5txlgQ6FnSSOn8_8uEQFbU6hzfaiFOLHE4A130_provenance.
- NP441561.RAZ0pjqFoj5txlgQ6FnSSOn8_8uEQFbU6hzfaiFOLHE4A130_assertion wasDerivedFrom befree-2016 NP441561.RAZ0pjqFoj5txlgQ6FnSSOn8_8uEQFbU6hzfaiFOLHE4A130_provenance.
- NP441561.RAZ0pjqFoj5txlgQ6FnSSOn8_8uEQFbU6hzfaiFOLHE4A130_assertion wasGeneratedBy ECO_0000203 NP441561.RAZ0pjqFoj5txlgQ6FnSSOn8_8uEQFbU6hzfaiFOLHE4A130_provenance.
- befree-2016 importedOn "2016-02-19" NP441561.RAZ0pjqFoj5txlgQ6FnSSOn8_8uEQFbU6hzfaiFOLHE4A130_provenance.