Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1245552.RAfLKRdvcUl2PMGuhWjacENgTWFKhAw-g8wHLzToHGfWo130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1245552.RAfLKRdvcUl2PMGuhWjacENgTWFKhAw-g8wHLzToHGfWo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1245552.RAfLKRdvcUl2PMGuhWjacENgTWFKhAw-g8wHLzToHGfWo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1245552.RAfLKRdvcUl2PMGuhWjacENgTWFKhAw-g8wHLzToHGfWo130_provenance.
- NP1245552.RAfLKRdvcUl2PMGuhWjacENgTWFKhAw-g8wHLzToHGfWo130_assertion description "[Most of mutations in the dystrophin gene were localized in the hot spots - different for deletions and duplications.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1245552.RAfLKRdvcUl2PMGuhWjacENgTWFKhAw-g8wHLzToHGfWo130_provenance.
- NP1245552.RAfLKRdvcUl2PMGuhWjacENgTWFKhAw-g8wHLzToHGfWo130_assertion evidence source_evidence_literature NP1245552.RAfLKRdvcUl2PMGuhWjacENgTWFKhAw-g8wHLzToHGfWo130_provenance.
- NP1245552.RAfLKRdvcUl2PMGuhWjacENgTWFKhAw-g8wHLzToHGfWo130_assertion SIO_000772 25482253 NP1245552.RAfLKRdvcUl2PMGuhWjacENgTWFKhAw-g8wHLzToHGfWo130_provenance.
- NP1245552.RAfLKRdvcUl2PMGuhWjacENgTWFKhAw-g8wHLzToHGfWo130_assertion wasDerivedFrom befree-2016 NP1245552.RAfLKRdvcUl2PMGuhWjacENgTWFKhAw-g8wHLzToHGfWo130_provenance.
- NP1245552.RAfLKRdvcUl2PMGuhWjacENgTWFKhAw-g8wHLzToHGfWo130_assertion wasGeneratedBy ECO_0000203 NP1245552.RAfLKRdvcUl2PMGuhWjacENgTWFKhAw-g8wHLzToHGfWo130_provenance.
- befree-2016 importedOn "2016-02-19" NP1245552.RAfLKRdvcUl2PMGuhWjacENgTWFKhAw-g8wHLzToHGfWo130_provenance.