Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP876066.RAZL-bbxnThwzru3u97vgMOXVvevBHl8AeXuEF8Gp44E4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP876066.RAZL-bbxnThwzru3u97vgMOXVvevBHl8AeXuEF8Gp44E4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP876066.RAZL-bbxnThwzru3u97vgMOXVvevBHl8AeXuEF8Gp44E4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP876066.RAZL-bbxnThwzru3u97vgMOXVvevBHl8AeXuEF8Gp44E4130_provenance.
- NP876066.RAZL-bbxnThwzru3u97vgMOXVvevBHl8AeXuEF8Gp44E4130_assertion description "[CSTB-deficient mice, produced by targeted disruption of the mouse Cstb gene, display a phenotype similar to the human disease, with progressive ataxia and myoclonic seizures.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP876066.RAZL-bbxnThwzru3u97vgMOXVvevBHl8AeXuEF8Gp44E4130_provenance.
- NP876066.RAZL-bbxnThwzru3u97vgMOXVvevBHl8AeXuEF8Gp44E4130_assertion evidence source_evidence_literature NP876066.RAZL-bbxnThwzru3u97vgMOXVvevBHl8AeXuEF8Gp44E4130_provenance.
- NP876066.RAZL-bbxnThwzru3u97vgMOXVvevBHl8AeXuEF8Gp44E4130_assertion SIO_000772 12853462 NP876066.RAZL-bbxnThwzru3u97vgMOXVvevBHl8AeXuEF8Gp44E4130_provenance.
- NP876066.RAZL-bbxnThwzru3u97vgMOXVvevBHl8AeXuEF8Gp44E4130_assertion wasDerivedFrom befree-20140225 NP876066.RAZL-bbxnThwzru3u97vgMOXVvevBHl8AeXuEF8Gp44E4130_provenance.
- NP876066.RAZL-bbxnThwzru3u97vgMOXVvevBHl8AeXuEF8Gp44E4130_assertion wasGeneratedBy ECO_0000203 NP876066.RAZL-bbxnThwzru3u97vgMOXVvevBHl8AeXuEF8Gp44E4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP876066.RAZL-bbxnThwzru3u97vgMOXVvevBHl8AeXuEF8Gp44E4130_provenance.