Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP420112.RAwOuNstBUtx85G5XDvyWZu07nXXihoM7RHQzu9lxd13M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP420112.RAwOuNstBUtx85G5XDvyWZu07nXXihoM7RHQzu9lxd13M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP420112.RAwOuNstBUtx85G5XDvyWZu07nXXihoM7RHQzu9lxd13M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP420112.RAwOuNstBUtx85G5XDvyWZu07nXXihoM7RHQzu9lxd13M130_provenance.
- NP420112.RAwOuNstBUtx85G5XDvyWZu07nXXihoM7RHQzu9lxd13M130_assertion description "[Recent evidence indicates that mutations in the gene encoding the WNK1 [with no K (lysine) protein kinase-1] results in an inherited hypertension syndrome called pseudohypoaldosteronism type II.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP420112.RAwOuNstBUtx85G5XDvyWZu07nXXihoM7RHQzu9lxd13M130_provenance.
- NP420112.RAwOuNstBUtx85G5XDvyWZu07nXXihoM7RHQzu9lxd13M130_assertion evidence source_evidence_literature NP420112.RAwOuNstBUtx85G5XDvyWZu07nXXihoM7RHQzu9lxd13M130_provenance.
- NP420112.RAwOuNstBUtx85G5XDvyWZu07nXXihoM7RHQzu9lxd13M130_assertion SIO_000772 14611643 NP420112.RAwOuNstBUtx85G5XDvyWZu07nXXihoM7RHQzu9lxd13M130_provenance.
- NP420112.RAwOuNstBUtx85G5XDvyWZu07nXXihoM7RHQzu9lxd13M130_assertion wasDerivedFrom befree-2016 NP420112.RAwOuNstBUtx85G5XDvyWZu07nXXihoM7RHQzu9lxd13M130_provenance.
- NP420112.RAwOuNstBUtx85G5XDvyWZu07nXXihoM7RHQzu9lxd13M130_assertion wasGeneratedBy ECO_0000203 NP420112.RAwOuNstBUtx85G5XDvyWZu07nXXihoM7RHQzu9lxd13M130_provenance.
- befree-2016 importedOn "2016-02-19" NP420112.RAwOuNstBUtx85G5XDvyWZu07nXXihoM7RHQzu9lxd13M130_provenance.