Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP169856.RA6SPIvAQ_HsLNaYvHzLYFP3KFmnOYEwLpmjcTWe6TmJE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP169856.RA6SPIvAQ_HsLNaYvHzLYFP3KFmnOYEwLpmjcTWe6TmJE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP169856.RA6SPIvAQ_HsLNaYvHzLYFP3KFmnOYEwLpmjcTWe6TmJE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP169856.RA6SPIvAQ_HsLNaYvHzLYFP3KFmnOYEwLpmjcTWe6TmJE130_provenance.
- NP169856.RA6SPIvAQ_HsLNaYvHzLYFP3KFmnOYEwLpmjcTWe6TmJE130_assertion description "[Expression of a mutant SOD1 typical of fALS patients restricted to either motor neurons or astrocytes is insufficient to generate a pathological phenotype in mouse models, suggesting that a deleterious interplay between different cell types is necessary for the pathogenesis of the disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP169856.RA6SPIvAQ_HsLNaYvHzLYFP3KFmnOYEwLpmjcTWe6TmJE130_provenance.
- NP169856.RA6SPIvAQ_HsLNaYvHzLYFP3KFmnOYEwLpmjcTWe6TmJE130_assertion evidence source_evidence_literature NP169856.RA6SPIvAQ_HsLNaYvHzLYFP3KFmnOYEwLpmjcTWe6TmJE130_provenance.
- NP169856.RA6SPIvAQ_HsLNaYvHzLYFP3KFmnOYEwLpmjcTWe6TmJE130_assertion SIO_000772 15208263 NP169856.RA6SPIvAQ_HsLNaYvHzLYFP3KFmnOYEwLpmjcTWe6TmJE130_provenance.
- NP169856.RA6SPIvAQ_HsLNaYvHzLYFP3KFmnOYEwLpmjcTWe6TmJE130_assertion wasDerivedFrom befree-20140225 NP169856.RA6SPIvAQ_HsLNaYvHzLYFP3KFmnOYEwLpmjcTWe6TmJE130_provenance.
- NP169856.RA6SPIvAQ_HsLNaYvHzLYFP3KFmnOYEwLpmjcTWe6TmJE130_assertion wasGeneratedBy ECO_0000203 NP169856.RA6SPIvAQ_HsLNaYvHzLYFP3KFmnOYEwLpmjcTWe6TmJE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP169856.RA6SPIvAQ_HsLNaYvHzLYFP3KFmnOYEwLpmjcTWe6TmJE130_provenance.