Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP938741.RAJwCVp004mxeHhcm6s23FkytxYfJCFbsYWPhtVGIQxIY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP938741.RAJwCVp004mxeHhcm6s23FkytxYfJCFbsYWPhtVGIQxIY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP938741.RAJwCVp004mxeHhcm6s23FkytxYfJCFbsYWPhtVGIQxIY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP938741.RAJwCVp004mxeHhcm6s23FkytxYfJCFbsYWPhtVGIQxIY130_provenance.
- NP938741.RAJwCVp004mxeHhcm6s23FkytxYfJCFbsYWPhtVGIQxIY130_assertion description "[To investigate the molecular pathways disrupted by dominant spastin mutations in apparently unaffected skeletal muscle from patients with motor neuron disease (SPG4).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP938741.RAJwCVp004mxeHhcm6s23FkytxYfJCFbsYWPhtVGIQxIY130_provenance.
- NP938741.RAJwCVp004mxeHhcm6s23FkytxYfJCFbsYWPhtVGIQxIY130_assertion evidence source_evidence_literature NP938741.RAJwCVp004mxeHhcm6s23FkytxYfJCFbsYWPhtVGIQxIY130_provenance.
- NP938741.RAJwCVp004mxeHhcm6s23FkytxYfJCFbsYWPhtVGIQxIY130_assertion SIO_000772 15079007 NP938741.RAJwCVp004mxeHhcm6s23FkytxYfJCFbsYWPhtVGIQxIY130_provenance.
- NP938741.RAJwCVp004mxeHhcm6s23FkytxYfJCFbsYWPhtVGIQxIY130_assertion wasDerivedFrom befree-20140225 NP938741.RAJwCVp004mxeHhcm6s23FkytxYfJCFbsYWPhtVGIQxIY130_provenance.
- NP938741.RAJwCVp004mxeHhcm6s23FkytxYfJCFbsYWPhtVGIQxIY130_assertion wasGeneratedBy ECO_0000203 NP938741.RAJwCVp004mxeHhcm6s23FkytxYfJCFbsYWPhtVGIQxIY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP938741.RAJwCVp004mxeHhcm6s23FkytxYfJCFbsYWPhtVGIQxIY130_provenance.