Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP792036.RAtFIiu0xeMn6WKUA6tJedybXawJAZSDekBxQBrZVRgpw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP792036.RAtFIiu0xeMn6WKUA6tJedybXawJAZSDekBxQBrZVRgpw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP792036.RAtFIiu0xeMn6WKUA6tJedybXawJAZSDekBxQBrZVRgpw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP792036.RAtFIiu0xeMn6WKUA6tJedybXawJAZSDekBxQBrZVRgpw130_provenance.
- NP792036.RAtFIiu0xeMn6WKUA6tJedybXawJAZSDekBxQBrZVRgpw130_assertion description "[The 3'-UTR contains a polymorphic AGG repeat that appears not to be expanded in patients suffering from different neurodegenerative disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP792036.RAtFIiu0xeMn6WKUA6tJedybXawJAZSDekBxQBrZVRgpw130_provenance.
- NP792036.RAtFIiu0xeMn6WKUA6tJedybXawJAZSDekBxQBrZVRgpw130_assertion evidence source_evidence_literature NP792036.RAtFIiu0xeMn6WKUA6tJedybXawJAZSDekBxQBrZVRgpw130_provenance.
- NP792036.RAtFIiu0xeMn6WKUA6tJedybXawJAZSDekBxQBrZVRgpw130_assertion SIO_000772 9811930 NP792036.RAtFIiu0xeMn6WKUA6tJedybXawJAZSDekBxQBrZVRgpw130_provenance.
- NP792036.RAtFIiu0xeMn6WKUA6tJedybXawJAZSDekBxQBrZVRgpw130_assertion wasDerivedFrom befree-20150227 NP792036.RAtFIiu0xeMn6WKUA6tJedybXawJAZSDekBxQBrZVRgpw130_provenance.
- NP792036.RAtFIiu0xeMn6WKUA6tJedybXawJAZSDekBxQBrZVRgpw130_assertion wasGeneratedBy ECO_0000203 NP792036.RAtFIiu0xeMn6WKUA6tJedybXawJAZSDekBxQBrZVRgpw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP792036.RAtFIiu0xeMn6WKUA6tJedybXawJAZSDekBxQBrZVRgpw130_provenance.