Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP660982.RAtkTWvFNjXHUgfDKO7kEV-lAeWrpDJ3TC3MZQgFXaa5A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP660982.RAtkTWvFNjXHUgfDKO7kEV-lAeWrpDJ3TC3MZQgFXaa5A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP660982.RAtkTWvFNjXHUgfDKO7kEV-lAeWrpDJ3TC3MZQgFXaa5A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP660982.RAtkTWvFNjXHUgfDKO7kEV-lAeWrpDJ3TC3MZQgFXaa5A130_provenance.
- NP660982.RAtkTWvFNjXHUgfDKO7kEV-lAeWrpDJ3TC3MZQgFXaa5A130_assertion description "[Two electrophoretic variants of haptoglobin in which the alpha 2 chain had more basic or more acidic spots were found in DMD patients with a rapidly progressing form of the disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP660982.RAtkTWvFNjXHUgfDKO7kEV-lAeWrpDJ3TC3MZQgFXaa5A130_provenance.
- NP660982.RAtkTWvFNjXHUgfDKO7kEV-lAeWrpDJ3TC3MZQgFXaa5A130_assertion evidence source_evidence_literature NP660982.RAtkTWvFNjXHUgfDKO7kEV-lAeWrpDJ3TC3MZQgFXaa5A130_provenance.
- NP660982.RAtkTWvFNjXHUgfDKO7kEV-lAeWrpDJ3TC3MZQgFXaa5A130_assertion SIO_000772 2776732 NP660982.RAtkTWvFNjXHUgfDKO7kEV-lAeWrpDJ3TC3MZQgFXaa5A130_provenance.
- NP660982.RAtkTWvFNjXHUgfDKO7kEV-lAeWrpDJ3TC3MZQgFXaa5A130_assertion wasDerivedFrom befree-20140225 NP660982.RAtkTWvFNjXHUgfDKO7kEV-lAeWrpDJ3TC3MZQgFXaa5A130_provenance.
- NP660982.RAtkTWvFNjXHUgfDKO7kEV-lAeWrpDJ3TC3MZQgFXaa5A130_assertion wasGeneratedBy ECO_0000203 NP660982.RAtkTWvFNjXHUgfDKO7kEV-lAeWrpDJ3TC3MZQgFXaa5A130_provenance.
- befree-20140225 importedOn "2014-02-25" NP660982.RAtkTWvFNjXHUgfDKO7kEV-lAeWrpDJ3TC3MZQgFXaa5A130_provenance.