Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP483348.RA-3d8kmc56-MzTzbXQBYXoK-kj4lvHcP5rR35ryUwSDE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP483348.RA-3d8kmc56-MzTzbXQBYXoK-kj4lvHcP5rR35ryUwSDE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP483348.RA-3d8kmc56-MzTzbXQBYXoK-kj4lvHcP5rR35ryUwSDE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP483348.RA-3d8kmc56-MzTzbXQBYXoK-kj4lvHcP5rR35ryUwSDE130_provenance.
- befree-2016 importedOn "2016-02-19" NP483348.RA-3d8kmc56-MzTzbXQBYXoK-kj4lvHcP5rR35ryUwSDE130_provenance.
- NP483348.RA-3d8kmc56-MzTzbXQBYXoK-kj4lvHcP5rR35ryUwSDE130_assertion wasGeneratedBy ECO_0000203 NP483348.RA-3d8kmc56-MzTzbXQBYXoK-kj4lvHcP5rR35ryUwSDE130_provenance.
- NP483348.RA-3d8kmc56-MzTzbXQBYXoK-kj4lvHcP5rR35ryUwSDE130_assertion wasDerivedFrom befree-2016 NP483348.RA-3d8kmc56-MzTzbXQBYXoK-kj4lvHcP5rR35ryUwSDE130_provenance.
- NP483348.RA-3d8kmc56-MzTzbXQBYXoK-kj4lvHcP5rR35ryUwSDE130_assertion SIO_000772 15741255 NP483348.RA-3d8kmc56-MzTzbXQBYXoK-kj4lvHcP5rR35ryUwSDE130_provenance.
- NP483348.RA-3d8kmc56-MzTzbXQBYXoK-kj4lvHcP5rR35ryUwSDE130_assertion evidence source_evidence_literature NP483348.RA-3d8kmc56-MzTzbXQBYXoK-kj4lvHcP5rR35ryUwSDE130_provenance.
- NP483348.RA-3d8kmc56-MzTzbXQBYXoK-kj4lvHcP5rR35ryUwSDE130_assertion description "[Although a fortuitous association cannot be excluded, HLRCC may be added to the short list of monogenic disorders that have been reported to be associated with the development of adrenal tumors; FH may be considered a candidate gene for MMAD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP483348.RA-3d8kmc56-MzTzbXQBYXoK-kj4lvHcP5rR35ryUwSDE130_provenance.