Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1317382.RA0QBxXVbA1qLor2WcTP4_4ievB-SfBhRTlnXx4QmrHmE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1317382.RA0QBxXVbA1qLor2WcTP4_4ievB-SfBhRTlnXx4QmrHmE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1317382.RA0QBxXVbA1qLor2WcTP4_4ievB-SfBhRTlnXx4QmrHmE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1317382.RA0QBxXVbA1qLor2WcTP4_4ievB-SfBhRTlnXx4QmrHmE130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP1317382.RA0QBxXVbA1qLor2WcTP4_4ievB-SfBhRTlnXx4QmrHmE130_provenance.