Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP208570.RAFxzgAquoqyM1HD3rU_So8ARBc3v6ParCoXffJl4AHDE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP208570.RAFxzgAquoqyM1HD3rU_So8ARBc3v6ParCoXffJl4AHDE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP208570.RAFxzgAquoqyM1HD3rU_So8ARBc3v6ParCoXffJl4AHDE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP208570.RAFxzgAquoqyM1HD3rU_So8ARBc3v6ParCoXffJl4AHDE130_provenance.
- NP208570.RAFxzgAquoqyM1HD3rU_So8ARBc3v6ParCoXffJl4AHDE130_assertion description "[Here, we compared the expression of sHSPs in transgenic mouse models of fALS, Parkinson's disease (PD), dentato-rubral pallido-luysian atrophy (DRPLA) and Huntington's disease (HD); where the expression of mutant cDNA genes was under the transcriptional regulation of the mouse prion protein promoter.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP208570.RAFxzgAquoqyM1HD3rU_So8ARBc3v6ParCoXffJl4AHDE130_provenance.
- NP208570.RAFxzgAquoqyM1HD3rU_So8ARBc3v6ParCoXffJl4AHDE130_assertion evidence source_evidence_literature NP208570.RAFxzgAquoqyM1HD3rU_So8ARBc3v6ParCoXffJl4AHDE130_provenance.
- NP208570.RAFxzgAquoqyM1HD3rU_So8ARBc3v6ParCoXffJl4AHDE130_assertion SIO_000772 17316906 NP208570.RAFxzgAquoqyM1HD3rU_So8ARBc3v6ParCoXffJl4AHDE130_provenance.
- NP208570.RAFxzgAquoqyM1HD3rU_So8ARBc3v6ParCoXffJl4AHDE130_assertion wasDerivedFrom befree-20140225 NP208570.RAFxzgAquoqyM1HD3rU_So8ARBc3v6ParCoXffJl4AHDE130_provenance.
- NP208570.RAFxzgAquoqyM1HD3rU_So8ARBc3v6ParCoXffJl4AHDE130_assertion wasGeneratedBy ECO_0000203 NP208570.RAFxzgAquoqyM1HD3rU_So8ARBc3v6ParCoXffJl4AHDE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP208570.RAFxzgAquoqyM1HD3rU_So8ARBc3v6ParCoXffJl4AHDE130_provenance.