Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP268729.RAWFOpJsVAG-d4TbHdeYpxXyarBHH0CroIspc1L5XmFIw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP268729.RAWFOpJsVAG-d4TbHdeYpxXyarBHH0CroIspc1L5XmFIw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP268729.RAWFOpJsVAG-d4TbHdeYpxXyarBHH0CroIspc1L5XmFIw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP268729.RAWFOpJsVAG-d4TbHdeYpxXyarBHH0CroIspc1L5XmFIw130_provenance.
- NP268729.RAWFOpJsVAG-d4TbHdeYpxXyarBHH0CroIspc1L5XmFIw130_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." NP268729.RAWFOpJsVAG-d4TbHdeYpxXyarBHH0CroIspc1L5XmFIw130_provenance.
- NP268729.RAWFOpJsVAG-d4TbHdeYpxXyarBHH0CroIspc1L5XmFIw130_assertion evidence source_evidence_literature NP268729.RAWFOpJsVAG-d4TbHdeYpxXyarBHH0CroIspc1L5XmFIw130_provenance.
- NP268729.RAWFOpJsVAG-d4TbHdeYpxXyarBHH0CroIspc1L5XmFIw130_assertion SIO_000772 21115159 NP268729.RAWFOpJsVAG-d4TbHdeYpxXyarBHH0CroIspc1L5XmFIw130_provenance.
- NP268729.RAWFOpJsVAG-d4TbHdeYpxXyarBHH0CroIspc1L5XmFIw130_assertion wasDerivedFrom befree-20140225 NP268729.RAWFOpJsVAG-d4TbHdeYpxXyarBHH0CroIspc1L5XmFIw130_provenance.
- NP268729.RAWFOpJsVAG-d4TbHdeYpxXyarBHH0CroIspc1L5XmFIw130_assertion wasGeneratedBy ECO_0000203 NP268729.RAWFOpJsVAG-d4TbHdeYpxXyarBHH0CroIspc1L5XmFIw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP268729.RAWFOpJsVAG-d4TbHdeYpxXyarBHH0CroIspc1L5XmFIw130_provenance.