Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP447571.RAVYu-8-Gh06fL1bnR-FcD0KeVoZZHIgaKI-gdcASsE-E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP447571.RAVYu-8-Gh06fL1bnR-FcD0KeVoZZHIgaKI-gdcASsE-E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP447571.RAVYu-8-Gh06fL1bnR-FcD0KeVoZZHIgaKI-gdcASsE-E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP447571.RAVYu-8-Gh06fL1bnR-FcD0KeVoZZHIgaKI-gdcASsE-E130_provenance.
- NP447571.RAVYu-8-Gh06fL1bnR-FcD0KeVoZZHIgaKI-gdcASsE-E130_assertion description "[Pseudohypoaldosteronism type II (PHA2) is a rare autosomal dominant form of volume-dependent low-renin hypertension characterized by hyperkalemia and hyperchloremic acidosis but also by a normal glomerular filtration rate.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP447571.RAVYu-8-Gh06fL1bnR-FcD0KeVoZZHIgaKI-gdcASsE-E130_provenance.
- NP447571.RAVYu-8-Gh06fL1bnR-FcD0KeVoZZHIgaKI-gdcASsE-E130_assertion evidence source_evidence_literature NP447571.RAVYu-8-Gh06fL1bnR-FcD0KeVoZZHIgaKI-gdcASsE-E130_provenance.
- NP447571.RAVYu-8-Gh06fL1bnR-FcD0KeVoZZHIgaKI-gdcASsE-E130_assertion SIO_000772 10869238 NP447571.RAVYu-8-Gh06fL1bnR-FcD0KeVoZZHIgaKI-gdcASsE-E130_provenance.
- NP447571.RAVYu-8-Gh06fL1bnR-FcD0KeVoZZHIgaKI-gdcASsE-E130_assertion wasDerivedFrom befree-20140225 NP447571.RAVYu-8-Gh06fL1bnR-FcD0KeVoZZHIgaKI-gdcASsE-E130_provenance.
- NP447571.RAVYu-8-Gh06fL1bnR-FcD0KeVoZZHIgaKI-gdcASsE-E130_assertion wasGeneratedBy ECO_0000203 NP447571.RAVYu-8-Gh06fL1bnR-FcD0KeVoZZHIgaKI-gdcASsE-E130_provenance.
- befree-20140225 importedOn "2014-02-25" NP447571.RAVYu-8-Gh06fL1bnR-FcD0KeVoZZHIgaKI-gdcASsE-E130_provenance.