Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP154869.RAmPCVarnoUQ5LKxrCyN8R_w_oZW-n9CyKSh6wPWwwa1M130_assertion> ?p ?o ?g. }
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- NP154869.RAmPCVarnoUQ5LKxrCyN8R_w_oZW-n9CyKSh6wPWwwa1M130_assertion type Assertion NP154869.RAmPCVarnoUQ5LKxrCyN8R_w_oZW-n9CyKSh6wPWwwa1M130_head.
- NP154869.RAmPCVarnoUQ5LKxrCyN8R_w_oZW-n9CyKSh6wPWwwa1M130_assertion description "[The apparent mineralocorticoid excess syndrome (AME) is a rare autosomal recessive disorder due to the deficiency of 11beta-hydroxysteroid dehydrogenase type 2 enzyme (11beta-HSD2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP154869.RAmPCVarnoUQ5LKxrCyN8R_w_oZW-n9CyKSh6wPWwwa1M130_provenance.
- NP154869.RAmPCVarnoUQ5LKxrCyN8R_w_oZW-n9CyKSh6wPWwwa1M130_assertion evidence source_evidence_literature NP154869.RAmPCVarnoUQ5LKxrCyN8R_w_oZW-n9CyKSh6wPWwwa1M130_provenance.
- NP154869.RAmPCVarnoUQ5LKxrCyN8R_w_oZW-n9CyKSh6wPWwwa1M130_assertion SIO_000772 19169481 NP154869.RAmPCVarnoUQ5LKxrCyN8R_w_oZW-n9CyKSh6wPWwwa1M130_provenance.
- NP154869.RAmPCVarnoUQ5LKxrCyN8R_w_oZW-n9CyKSh6wPWwwa1M130_assertion wasDerivedFrom befree-20140225 NP154869.RAmPCVarnoUQ5LKxrCyN8R_w_oZW-n9CyKSh6wPWwwa1M130_provenance.
- NP154869.RAmPCVarnoUQ5LKxrCyN8R_w_oZW-n9CyKSh6wPWwwa1M130_assertion wasGeneratedBy ECO_0000203 NP154869.RAmPCVarnoUQ5LKxrCyN8R_w_oZW-n9CyKSh6wPWwwa1M130_provenance.