Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP887239.RABUUy7fnKsX2XWD3ZlH-aSKlGqFAOiFrfDP-3ZtCbOPc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP887239.RABUUy7fnKsX2XWD3ZlH-aSKlGqFAOiFrfDP-3ZtCbOPc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP887239.RABUUy7fnKsX2XWD3ZlH-aSKlGqFAOiFrfDP-3ZtCbOPc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP887239.RABUUy7fnKsX2XWD3ZlH-aSKlGqFAOiFrfDP-3ZtCbOPc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP887239.RABUUy7fnKsX2XWD3ZlH-aSKlGqFAOiFrfDP-3ZtCbOPc130_provenance.
- NP887239.RABUUy7fnKsX2XWD3ZlH-aSKlGqFAOiFrfDP-3ZtCbOPc130_assertion wasGeneratedBy ECO_0000203 NP887239.RABUUy7fnKsX2XWD3ZlH-aSKlGqFAOiFrfDP-3ZtCbOPc130_provenance.
- NP887239.RABUUy7fnKsX2XWD3ZlH-aSKlGqFAOiFrfDP-3ZtCbOPc130_assertion wasDerivedFrom befree-20150227 NP887239.RABUUy7fnKsX2XWD3ZlH-aSKlGqFAOiFrfDP-3ZtCbOPc130_provenance.
- NP887239.RABUUy7fnKsX2XWD3ZlH-aSKlGqFAOiFrfDP-3ZtCbOPc130_assertion SIO_000772 24502382 NP887239.RABUUy7fnKsX2XWD3ZlH-aSKlGqFAOiFrfDP-3ZtCbOPc130_provenance.
- NP887239.RABUUy7fnKsX2XWD3ZlH-aSKlGqFAOiFrfDP-3ZtCbOPc130_assertion evidence source_evidence_literature NP887239.RABUUy7fnKsX2XWD3ZlH-aSKlGqFAOiFrfDP-3ZtCbOPc130_provenance.
- NP887239.RABUUy7fnKsX2XWD3ZlH-aSKlGqFAOiFrfDP-3ZtCbOPc130_assertion description "[The recent identification of causal mutations and polymorphisms in COQ2, a gene encoding a biosynthetic enzyme for the production of the lipid-soluble electron carrier coenzyme Q10 (ubiquinone), puts membrane transporters as central to MSA pathogenesis, although how such transporters are involved in the early myelin degeneration observed in MSA remains unclear.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP887239.RABUUy7fnKsX2XWD3ZlH-aSKlGqFAOiFrfDP-3ZtCbOPc130_provenance.