Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP256124.RA95FO5tDP-FpIo25pcmGmNIDKrbgfFi4jxql5DAUfdQc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP256124.RA95FO5tDP-FpIo25pcmGmNIDKrbgfFi4jxql5DAUfdQc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP256124.RA95FO5tDP-FpIo25pcmGmNIDKrbgfFi4jxql5DAUfdQc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP256124.RA95FO5tDP-FpIo25pcmGmNIDKrbgfFi4jxql5DAUfdQc130_provenance.
- NP256124.RA95FO5tDP-FpIo25pcmGmNIDKrbgfFi4jxql5DAUfdQc130_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." NP256124.RA95FO5tDP-FpIo25pcmGmNIDKrbgfFi4jxql5DAUfdQc130_provenance.
- NP256124.RA95FO5tDP-FpIo25pcmGmNIDKrbgfFi4jxql5DAUfdQc130_assertion evidence source_evidence_literature NP256124.RA95FO5tDP-FpIo25pcmGmNIDKrbgfFi4jxql5DAUfdQc130_provenance.
- NP256124.RA95FO5tDP-FpIo25pcmGmNIDKrbgfFi4jxql5DAUfdQc130_assertion SIO_000772 15866321 NP256124.RA95FO5tDP-FpIo25pcmGmNIDKrbgfFi4jxql5DAUfdQc130_provenance.
- NP256124.RA95FO5tDP-FpIo25pcmGmNIDKrbgfFi4jxql5DAUfdQc130_assertion wasDerivedFrom befree-20140225 NP256124.RA95FO5tDP-FpIo25pcmGmNIDKrbgfFi4jxql5DAUfdQc130_provenance.
- NP256124.RA95FO5tDP-FpIo25pcmGmNIDKrbgfFi4jxql5DAUfdQc130_assertion wasGeneratedBy ECO_0000203 NP256124.RA95FO5tDP-FpIo25pcmGmNIDKrbgfFi4jxql5DAUfdQc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP256124.RA95FO5tDP-FpIo25pcmGmNIDKrbgfFi4jxql5DAUfdQc130_provenance.