Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP524487.RAXUmfEVG6-dx98tvqyLDdLhCX-o8xarJn3Fq2_yoT-KQ130_assertion> ?p ?o ?g. }
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- NP524487.RAXUmfEVG6-dx98tvqyLDdLhCX-o8xarJn3Fq2_yoT-KQ130_assertion type Assertion NP524487.RAXUmfEVG6-dx98tvqyLDdLhCX-o8xarJn3Fq2_yoT-KQ130_head.
- NP524487.RAXUmfEVG6-dx98tvqyLDdLhCX-o8xarJn3Fq2_yoT-KQ130_assertion wasGeneratedBy ECO_0000203 NP524487.RAXUmfEVG6-dx98tvqyLDdLhCX-o8xarJn3Fq2_yoT-KQ130_provenance.
- NP524487.RAXUmfEVG6-dx98tvqyLDdLhCX-o8xarJn3Fq2_yoT-KQ130_assertion wasDerivedFrom befree-20140225 NP524487.RAXUmfEVG6-dx98tvqyLDdLhCX-o8xarJn3Fq2_yoT-KQ130_provenance.
- NP524487.RAXUmfEVG6-dx98tvqyLDdLhCX-o8xarJn3Fq2_yoT-KQ130_assertion SIO_000772 22964742 NP524487.RAXUmfEVG6-dx98tvqyLDdLhCX-o8xarJn3Fq2_yoT-KQ130_provenance.
- NP524487.RAXUmfEVG6-dx98tvqyLDdLhCX-o8xarJn3Fq2_yoT-KQ130_assertion evidence source_evidence_literature NP524487.RAXUmfEVG6-dx98tvqyLDdLhCX-o8xarJn3Fq2_yoT-KQ130_provenance.
- NP524487.RAXUmfEVG6-dx98tvqyLDdLhCX-o8xarJn3Fq2_yoT-KQ130_assertion description "[11β-Hydroxylase deficiency (11β-OHD), caused by CYP11B1 mutations, is characterized by hyporeninemic, hypokalemic hypertension and hyperandrogenism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP524487.RAXUmfEVG6-dx98tvqyLDdLhCX-o8xarJn3Fq2_yoT-KQ130_provenance.