Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1001001.RAiX287OBIT7jWYhuteE-Nc6zFLIcfbspu3VP9iGQx6w0130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1001001.RAiX287OBIT7jWYhuteE-Nc6zFLIcfbspu3VP9iGQx6w0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1001001.RAiX287OBIT7jWYhuteE-Nc6zFLIcfbspu3VP9iGQx6w0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1001001.RAiX287OBIT7jWYhuteE-Nc6zFLIcfbspu3VP9iGQx6w0130_provenance.
- NP1001001.RAiX287OBIT7jWYhuteE-Nc6zFLIcfbspu3VP9iGQx6w0130_assertion description "[This region contains the genes of FAM84A, NBAS, DDX1, MYCNOS and MYCN, of which haploinsufficiency or mutations of the MYCN gene is associated with Feingold syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1001001.RAiX287OBIT7jWYhuteE-Nc6zFLIcfbspu3VP9iGQx6w0130_provenance.
- NP1001001.RAiX287OBIT7jWYhuteE-Nc6zFLIcfbspu3VP9iGQx6w0130_assertion evidence source_evidence_literature NP1001001.RAiX287OBIT7jWYhuteE-Nc6zFLIcfbspu3VP9iGQx6w0130_provenance.
- NP1001001.RAiX287OBIT7jWYhuteE-Nc6zFLIcfbspu3VP9iGQx6w0130_assertion SIO_000772 22842076 NP1001001.RAiX287OBIT7jWYhuteE-Nc6zFLIcfbspu3VP9iGQx6w0130_provenance.
- NP1001001.RAiX287OBIT7jWYhuteE-Nc6zFLIcfbspu3VP9iGQx6w0130_assertion wasDerivedFrom befree-2016 NP1001001.RAiX287OBIT7jWYhuteE-Nc6zFLIcfbspu3VP9iGQx6w0130_provenance.
- NP1001001.RAiX287OBIT7jWYhuteE-Nc6zFLIcfbspu3VP9iGQx6w0130_assertion wasGeneratedBy ECO_0000203 NP1001001.RAiX287OBIT7jWYhuteE-Nc6zFLIcfbspu3VP9iGQx6w0130_provenance.
- befree-2016 importedOn "2016-02-19" NP1001001.RAiX287OBIT7jWYhuteE-Nc6zFLIcfbspu3VP9iGQx6w0130_provenance.