Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP946604.RAXotE-1fUtyJdnbAvWlI66Ysv9ZtOEGXlg2At6ORGumY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP946604.RAXotE-1fUtyJdnbAvWlI66Ysv9ZtOEGXlg2At6ORGumY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP946604.RAXotE-1fUtyJdnbAvWlI66Ysv9ZtOEGXlg2At6ORGumY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP946604.RAXotE-1fUtyJdnbAvWlI66Ysv9ZtOEGXlg2At6ORGumY130_provenance.
- NP946604.RAXotE-1fUtyJdnbAvWlI66Ysv9ZtOEGXlg2At6ORGumY130_assertion description "[Mutations in UBQLN2 encoding ubiquilin-2 have recently been identified in families with dominant X-linked juvenile and adult-onset amyotrophic lateral sclerosis (ALS) and ALS/dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP946604.RAXotE-1fUtyJdnbAvWlI66Ysv9ZtOEGXlg2At6ORGumY130_provenance.
- NP946604.RAXotE-1fUtyJdnbAvWlI66Ysv9ZtOEGXlg2At6ORGumY130_assertion evidence source_evidence_literature NP946604.RAXotE-1fUtyJdnbAvWlI66Ysv9ZtOEGXlg2At6ORGumY130_provenance.
- NP946604.RAXotE-1fUtyJdnbAvWlI66Ysv9ZtOEGXlg2At6ORGumY130_assertion SIO_000772 22169395 NP946604.RAXotE-1fUtyJdnbAvWlI66Ysv9ZtOEGXlg2At6ORGumY130_provenance.
- NP946604.RAXotE-1fUtyJdnbAvWlI66Ysv9ZtOEGXlg2At6ORGumY130_assertion wasDerivedFrom befree-2016 NP946604.RAXotE-1fUtyJdnbAvWlI66Ysv9ZtOEGXlg2At6ORGumY130_provenance.
- NP946604.RAXotE-1fUtyJdnbAvWlI66Ysv9ZtOEGXlg2At6ORGumY130_assertion wasGeneratedBy ECO_0000203 NP946604.RAXotE-1fUtyJdnbAvWlI66Ysv9ZtOEGXlg2At6ORGumY130_provenance.
- befree-2016 importedOn "2016-02-19" NP946604.RAXotE-1fUtyJdnbAvWlI66Ysv9ZtOEGXlg2At6ORGumY130_provenance.