Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1378028.RA0mL1ngQ9qcsZjnDlQRiGcSYCviwRumbAPG7H7aDeS08130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1378028.RA0mL1ngQ9qcsZjnDlQRiGcSYCviwRumbAPG7H7aDeS08130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1378028.RA0mL1ngQ9qcsZjnDlQRiGcSYCviwRumbAPG7H7aDeS08130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1378028.RA0mL1ngQ9qcsZjnDlQRiGcSYCviwRumbAPG7H7aDeS08130_provenance.
- NP1378028.RA0mL1ngQ9qcsZjnDlQRiGcSYCviwRumbAPG7H7aDeS08130_assertion description "[Mutations generating inactive enzymes have been described in the HSD11B2 gene in the congenital syndrome of apparent mineralocorticoid excess (AME)--a low renin form of hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1378028.RA0mL1ngQ9qcsZjnDlQRiGcSYCviwRumbAPG7H7aDeS08130_provenance.
- NP1378028.RA0mL1ngQ9qcsZjnDlQRiGcSYCviwRumbAPG7H7aDeS08130_assertion evidence source_evidence_literature NP1378028.RA0mL1ngQ9qcsZjnDlQRiGcSYCviwRumbAPG7H7aDeS08130_provenance.
- NP1378028.RA0mL1ngQ9qcsZjnDlQRiGcSYCviwRumbAPG7H7aDeS08130_assertion SIO_000772 9247735 NP1378028.RA0mL1ngQ9qcsZjnDlQRiGcSYCviwRumbAPG7H7aDeS08130_provenance.
- NP1378028.RA0mL1ngQ9qcsZjnDlQRiGcSYCviwRumbAPG7H7aDeS08130_assertion wasDerivedFrom befree-2016 NP1378028.RA0mL1ngQ9qcsZjnDlQRiGcSYCviwRumbAPG7H7aDeS08130_provenance.
- NP1378028.RA0mL1ngQ9qcsZjnDlQRiGcSYCviwRumbAPG7H7aDeS08130_assertion wasGeneratedBy ECO_0000203 NP1378028.RA0mL1ngQ9qcsZjnDlQRiGcSYCviwRumbAPG7H7aDeS08130_provenance.
- befree-2016 importedOn "2016-02-19" NP1378028.RA0mL1ngQ9qcsZjnDlQRiGcSYCviwRumbAPG7H7aDeS08130_provenance.