Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP624794.RA6jw_p22UYr_orkS0nGv87EvL7swXcJHeBHXzh0J9I0U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP624794.RA6jw_p22UYr_orkS0nGv87EvL7swXcJHeBHXzh0J9I0U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP624794.RA6jw_p22UYr_orkS0nGv87EvL7swXcJHeBHXzh0J9I0U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP624794.RA6jw_p22UYr_orkS0nGv87EvL7swXcJHeBHXzh0J9I0U130_provenance.
- NP624794.RA6jw_p22UYr_orkS0nGv87EvL7swXcJHeBHXzh0J9I0U130_assertion description "[Phosphodiesterase-11A (the PDE11A gene) and -8B (the PDE8B gene) mutations were found in patients with isolated adrenal hyperplasia and Cushing syndrome, as well in patients with PPNAD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP624794.RA6jw_p22UYr_orkS0nGv87EvL7swXcJHeBHXzh0J9I0U130_provenance.
- NP624794.RA6jw_p22UYr_orkS0nGv87EvL7swXcJHeBHXzh0J9I0U130_assertion evidence source_evidence_literature NP624794.RA6jw_p22UYr_orkS0nGv87EvL7swXcJHeBHXzh0J9I0U130_provenance.
- NP624794.RA6jw_p22UYr_orkS0nGv87EvL7swXcJHeBHXzh0J9I0U130_assertion SIO_000772 19063937 NP624794.RA6jw_p22UYr_orkS0nGv87EvL7swXcJHeBHXzh0J9I0U130_provenance.
- NP624794.RA6jw_p22UYr_orkS0nGv87EvL7swXcJHeBHXzh0J9I0U130_assertion wasDerivedFrom befree-20140225 NP624794.RA6jw_p22UYr_orkS0nGv87EvL7swXcJHeBHXzh0J9I0U130_provenance.
- NP624794.RA6jw_p22UYr_orkS0nGv87EvL7swXcJHeBHXzh0J9I0U130_assertion wasGeneratedBy ECO_0000203 NP624794.RA6jw_p22UYr_orkS0nGv87EvL7swXcJHeBHXzh0J9I0U130_provenance.
- befree-20140225 importedOn "2014-02-25" NP624794.RA6jw_p22UYr_orkS0nGv87EvL7swXcJHeBHXzh0J9I0U130_provenance.