Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP858191.RA2bCpmyJXxMqIfPGP4CYaWaWHFKWyCElhwc1lJ5bejjw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP858191.RA2bCpmyJXxMqIfPGP4CYaWaWHFKWyCElhwc1lJ5bejjw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP858191.RA2bCpmyJXxMqIfPGP4CYaWaWHFKWyCElhwc1lJ5bejjw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP858191.RA2bCpmyJXxMqIfPGP4CYaWaWHFKWyCElhwc1lJ5bejjw130_provenance.
- NP858191.RA2bCpmyJXxMqIfPGP4CYaWaWHFKWyCElhwc1lJ5bejjw130_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." NP858191.RA2bCpmyJXxMqIfPGP4CYaWaWHFKWyCElhwc1lJ5bejjw130_provenance.
- NP858191.RA2bCpmyJXxMqIfPGP4CYaWaWHFKWyCElhwc1lJ5bejjw130_assertion evidence source_evidence_literature NP858191.RA2bCpmyJXxMqIfPGP4CYaWaWHFKWyCElhwc1lJ5bejjw130_provenance.
- NP858191.RA2bCpmyJXxMqIfPGP4CYaWaWHFKWyCElhwc1lJ5bejjw130_assertion SIO_000772 7670488 NP858191.RA2bCpmyJXxMqIfPGP4CYaWaWHFKWyCElhwc1lJ5bejjw130_provenance.
- NP858191.RA2bCpmyJXxMqIfPGP4CYaWaWHFKWyCElhwc1lJ5bejjw130_assertion wasDerivedFrom befree-20140225 NP858191.RA2bCpmyJXxMqIfPGP4CYaWaWHFKWyCElhwc1lJ5bejjw130_provenance.
- NP858191.RA2bCpmyJXxMqIfPGP4CYaWaWHFKWyCElhwc1lJ5bejjw130_assertion wasGeneratedBy ECO_0000203 NP858191.RA2bCpmyJXxMqIfPGP4CYaWaWHFKWyCElhwc1lJ5bejjw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP858191.RA2bCpmyJXxMqIfPGP4CYaWaWHFKWyCElhwc1lJ5bejjw130_provenance.