Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP862255.RAqorptwlP82ucY0Lt4gL3Gk3uOUllUxJl7hfP26sYoEw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP862255.RAqorptwlP82ucY0Lt4gL3Gk3uOUllUxJl7hfP26sYoEw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP862255.RAqorptwlP82ucY0Lt4gL3Gk3uOUllUxJl7hfP26sYoEw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP862255.RAqorptwlP82ucY0Lt4gL3Gk3uOUllUxJl7hfP26sYoEw130_provenance.
- NP862255.RAqorptwlP82ucY0Lt4gL3Gk3uOUllUxJl7hfP26sYoEw130_assertion description "[This article comparatively reviews the experimental and human tissue-based evidence for the involvement of such mechanisms in neuronal death associated with the motor system disorders of X-linked spinobulbar muscular atrophy (SBMA; Kennedy's disease) and amyotrophic lateral sclerosis (ALS), especially disease related to mutations in the superoxide dismutase (SOD1) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP862255.RAqorptwlP82ucY0Lt4gL3Gk3uOUllUxJl7hfP26sYoEw130_provenance.
- NP862255.RAqorptwlP82ucY0Lt4gL3Gk3uOUllUxJl7hfP26sYoEw130_assertion evidence source_evidence_literature NP862255.RAqorptwlP82ucY0Lt4gL3Gk3uOUllUxJl7hfP26sYoEw130_provenance.
- NP862255.RAqorptwlP82ucY0Lt4gL3Gk3uOUllUxJl7hfP26sYoEw130_assertion SIO_000772 14636160 NP862255.RAqorptwlP82ucY0Lt4gL3Gk3uOUllUxJl7hfP26sYoEw130_provenance.
- NP862255.RAqorptwlP82ucY0Lt4gL3Gk3uOUllUxJl7hfP26sYoEw130_assertion wasDerivedFrom befree-20140225 NP862255.RAqorptwlP82ucY0Lt4gL3Gk3uOUllUxJl7hfP26sYoEw130_provenance.
- NP862255.RAqorptwlP82ucY0Lt4gL3Gk3uOUllUxJl7hfP26sYoEw130_assertion wasGeneratedBy ECO_0000203 NP862255.RAqorptwlP82ucY0Lt4gL3Gk3uOUllUxJl7hfP26sYoEw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP862255.RAqorptwlP82ucY0Lt4gL3Gk3uOUllUxJl7hfP26sYoEw130_provenance.