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- source_evidence_literature type ECO_0000212 NP1238557.RAnw0-ax00C_215EgnCg_afqGGP_-6o5bBjDeZBChOut8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1238557.RAnw0-ax00C_215EgnCg_afqGGP_-6o5bBjDeZBChOut8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1238557.RAnw0-ax00C_215EgnCg_afqGGP_-6o5bBjDeZBChOut8130_provenance.
- NP1238557.RAnw0-ax00C_215EgnCg_afqGGP_-6o5bBjDeZBChOut8130_assertion description "[Its mutant form, P56S-VAPB, which has been linked to a dominantly inherited form of Amyotrophic Lateral Sclerosis (ALS8), generates intracellular inclusions consisting in restructured ER domains whose role in ALS pathogenesis has not been elucidated.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1238557.RAnw0-ax00C_215EgnCg_afqGGP_-6o5bBjDeZBChOut8130_provenance.
- NP1238557.RAnw0-ax00C_215EgnCg_afqGGP_-6o5bBjDeZBChOut8130_assertion evidence source_evidence_literature NP1238557.RAnw0-ax00C_215EgnCg_afqGGP_-6o5bBjDeZBChOut8130_provenance.
- NP1238557.RAnw0-ax00C_215EgnCg_afqGGP_-6o5bBjDeZBChOut8130_assertion SIO_000772 25409455 NP1238557.RAnw0-ax00C_215EgnCg_afqGGP_-6o5bBjDeZBChOut8130_provenance.
- NP1238557.RAnw0-ax00C_215EgnCg_afqGGP_-6o5bBjDeZBChOut8130_assertion wasDerivedFrom befree-2016 NP1238557.RAnw0-ax00C_215EgnCg_afqGGP_-6o5bBjDeZBChOut8130_provenance.
- NP1238557.RAnw0-ax00C_215EgnCg_afqGGP_-6o5bBjDeZBChOut8130_assertion wasGeneratedBy ECO_0000203 NP1238557.RAnw0-ax00C_215EgnCg_afqGGP_-6o5bBjDeZBChOut8130_provenance.
- befree-2016 importedOn "2016-02-19" NP1238557.RAnw0-ax00C_215EgnCg_afqGGP_-6o5bBjDeZBChOut8130_provenance.