Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP421884.RASMvB_T0a1NQs99jTWvjNkMC4rNiAX77FQgtflvqux9g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP421884.RASMvB_T0a1NQs99jTWvjNkMC4rNiAX77FQgtflvqux9g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP421884.RASMvB_T0a1NQs99jTWvjNkMC4rNiAX77FQgtflvqux9g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP421884.RASMvB_T0a1NQs99jTWvjNkMC4rNiAX77FQgtflvqux9g130_provenance.
- NP421884.RASMvB_T0a1NQs99jTWvjNkMC4rNiAX77FQgtflvqux9g130_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." NP421884.RASMvB_T0a1NQs99jTWvjNkMC4rNiAX77FQgtflvqux9g130_provenance.
- NP421884.RASMvB_T0a1NQs99jTWvjNkMC4rNiAX77FQgtflvqux9g130_assertion evidence source_evidence_literature NP421884.RASMvB_T0a1NQs99jTWvjNkMC4rNiAX77FQgtflvqux9g130_provenance.
- NP421884.RASMvB_T0a1NQs99jTWvjNkMC4rNiAX77FQgtflvqux9g130_assertion SIO_000772 14636160 NP421884.RASMvB_T0a1NQs99jTWvjNkMC4rNiAX77FQgtflvqux9g130_provenance.
- NP421884.RASMvB_T0a1NQs99jTWvjNkMC4rNiAX77FQgtflvqux9g130_assertion wasDerivedFrom befree-2016 NP421884.RASMvB_T0a1NQs99jTWvjNkMC4rNiAX77FQgtflvqux9g130_provenance.
- NP421884.RASMvB_T0a1NQs99jTWvjNkMC4rNiAX77FQgtflvqux9g130_assertion wasGeneratedBy ECO_0000203 NP421884.RASMvB_T0a1NQs99jTWvjNkMC4rNiAX77FQgtflvqux9g130_provenance.
- befree-2016 importedOn "2016-02-19" NP421884.RASMvB_T0a1NQs99jTWvjNkMC4rNiAX77FQgtflvqux9g130_provenance.