Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP154869.RAmPCVarnoUQ5LKxrCyN8R_w_oZW-n9CyKSh6wPWwwa1M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP154869.RAmPCVarnoUQ5LKxrCyN8R_w_oZW-n9CyKSh6wPWwwa1M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP154869.RAmPCVarnoUQ5LKxrCyN8R_w_oZW-n9CyKSh6wPWwwa1M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP154869.RAmPCVarnoUQ5LKxrCyN8R_w_oZW-n9CyKSh6wPWwwa1M130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP154869.RAmPCVarnoUQ5LKxrCyN8R_w_oZW-n9CyKSh6wPWwwa1M130_provenance.