Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP267356.RATedLpzxSfmfK-tunXigPu7m2RoaVR58NIN_zgK1Bx2w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP267356.RATedLpzxSfmfK-tunXigPu7m2RoaVR58NIN_zgK1Bx2w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP267356.RATedLpzxSfmfK-tunXigPu7m2RoaVR58NIN_zgK1Bx2w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP267356.RATedLpzxSfmfK-tunXigPu7m2RoaVR58NIN_zgK1Bx2w130_provenance.
- NP267356.RATedLpzxSfmfK-tunXigPu7m2RoaVR58NIN_zgK1Bx2w130_assertion description "[Familial hyperaldosteronism type I(FH-I) In FH-I, inheritance of a 'hybrid' 11beta-hydroxylase/aldosterone synthase gene causes adrenocorticotrophic hormone (ACTH)-regulated aldosterone and 'hybrid steroid' (18hydroxy-cortisol and 18-oxo-cortisol) overproduction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP267356.RATedLpzxSfmfK-tunXigPu7m2RoaVR58NIN_zgK1Bx2w130_provenance.
- NP267356.RATedLpzxSfmfK-tunXigPu7m2RoaVR58NIN_zgK1Bx2w130_assertion evidence source_evidence_literature NP267356.RATedLpzxSfmfK-tunXigPu7m2RoaVR58NIN_zgK1Bx2w130_provenance.
- NP267356.RATedLpzxSfmfK-tunXigPu7m2RoaVR58NIN_zgK1Bx2w130_assertion SIO_000772 10994747 NP267356.RATedLpzxSfmfK-tunXigPu7m2RoaVR58NIN_zgK1Bx2w130_provenance.
- NP267356.RATedLpzxSfmfK-tunXigPu7m2RoaVR58NIN_zgK1Bx2w130_assertion wasDerivedFrom befree-20140225 NP267356.RATedLpzxSfmfK-tunXigPu7m2RoaVR58NIN_zgK1Bx2w130_provenance.
- NP267356.RATedLpzxSfmfK-tunXigPu7m2RoaVR58NIN_zgK1Bx2w130_assertion wasGeneratedBy ECO_0000203 NP267356.RATedLpzxSfmfK-tunXigPu7m2RoaVR58NIN_zgK1Bx2w130_provenance.
- befree-20140225 importedOn "2014-02-25" NP267356.RATedLpzxSfmfK-tunXigPu7m2RoaVR58NIN_zgK1Bx2w130_provenance.