Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1245979.RAMS5qkY6cWu6173BXAhBt1KgNIsSIU9cRrSF1Ba6J-YI130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1245979.RAMS5qkY6cWu6173BXAhBt1KgNIsSIU9cRrSF1Ba6J-YI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1245979.RAMS5qkY6cWu6173BXAhBt1KgNIsSIU9cRrSF1Ba6J-YI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1245979.RAMS5qkY6cWu6173BXAhBt1KgNIsSIU9cRrSF1Ba6J-YI130_provenance.
- NP1245979.RAMS5qkY6cWu6173BXAhBt1KgNIsSIU9cRrSF1Ba6J-YI130_assertion description "[In summary, our data show that dominant mutations in USP8 cause Cushing's disease via activation of EGF receptor signaling.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1245979.RAMS5qkY6cWu6173BXAhBt1KgNIsSIU9cRrSF1Ba6J-YI130_provenance.
- NP1245979.RAMS5qkY6cWu6173BXAhBt1KgNIsSIU9cRrSF1Ba6J-YI130_assertion evidence source_evidence_literature NP1245979.RAMS5qkY6cWu6173BXAhBt1KgNIsSIU9cRrSF1Ba6J-YI130_provenance.
- NP1245979.RAMS5qkY6cWu6173BXAhBt1KgNIsSIU9cRrSF1Ba6J-YI130_assertion SIO_000772 25485838 NP1245979.RAMS5qkY6cWu6173BXAhBt1KgNIsSIU9cRrSF1Ba6J-YI130_provenance.
- NP1245979.RAMS5qkY6cWu6173BXAhBt1KgNIsSIU9cRrSF1Ba6J-YI130_assertion wasDerivedFrom befree-2016 NP1245979.RAMS5qkY6cWu6173BXAhBt1KgNIsSIU9cRrSF1Ba6J-YI130_provenance.
- NP1245979.RAMS5qkY6cWu6173BXAhBt1KgNIsSIU9cRrSF1Ba6J-YI130_assertion wasGeneratedBy ECO_0000203 NP1245979.RAMS5qkY6cWu6173BXAhBt1KgNIsSIU9cRrSF1Ba6J-YI130_provenance.
- befree-2016 importedOn "2016-02-19" NP1245979.RAMS5qkY6cWu6173BXAhBt1KgNIsSIU9cRrSF1Ba6J-YI130_provenance.