Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1317382.RA0QBxXVbA1qLor2WcTP4_4ievB-SfBhRTlnXx4QmrHmE130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1317382.RA0QBxXVbA1qLor2WcTP4_4ievB-SfBhRTlnXx4QmrHmE130_assertion type Assertion NP1317382.RA0QBxXVbA1qLor2WcTP4_4ievB-SfBhRTlnXx4QmrHmE130_head.
- NP1317382.RA0QBxXVbA1qLor2WcTP4_4ievB-SfBhRTlnXx4QmrHmE130_assertion description "[The syndrome of apparent mineralocorticoid excess (AME) is an inherited form of human hypertension thought to result from a deficiency of 11 beta-hydroxysteroid dehydrogenase (11 beta HSD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1317382.RA0QBxXVbA1qLor2WcTP4_4ievB-SfBhRTlnXx4QmrHmE130_provenance.
- NP1317382.RA0QBxXVbA1qLor2WcTP4_4ievB-SfBhRTlnXx4QmrHmE130_assertion evidence source_evidence_literature NP1317382.RA0QBxXVbA1qLor2WcTP4_4ievB-SfBhRTlnXx4QmrHmE130_provenance.
- NP1317382.RA0QBxXVbA1qLor2WcTP4_4ievB-SfBhRTlnXx4QmrHmE130_assertion SIO_000772 7670488 NP1317382.RA0QBxXVbA1qLor2WcTP4_4ievB-SfBhRTlnXx4QmrHmE130_provenance.
- NP1317382.RA0QBxXVbA1qLor2WcTP4_4ievB-SfBhRTlnXx4QmrHmE130_assertion wasDerivedFrom befree-2016 NP1317382.RA0QBxXVbA1qLor2WcTP4_4ievB-SfBhRTlnXx4QmrHmE130_provenance.
- NP1317382.RA0QBxXVbA1qLor2WcTP4_4ievB-SfBhRTlnXx4QmrHmE130_assertion wasGeneratedBy ECO_0000203 NP1317382.RA0QBxXVbA1qLor2WcTP4_4ievB-SfBhRTlnXx4QmrHmE130_provenance.