Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP415746.RAx4SlGc-vHiWaTB9p1ouMyOb8GVVQNLfE1ttPBiHMy3M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP415746.RAx4SlGc-vHiWaTB9p1ouMyOb8GVVQNLfE1ttPBiHMy3M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP415746.RAx4SlGc-vHiWaTB9p1ouMyOb8GVVQNLfE1ttPBiHMy3M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP415746.RAx4SlGc-vHiWaTB9p1ouMyOb8GVVQNLfE1ttPBiHMy3M130_provenance.
- NP415746.RAx4SlGc-vHiWaTB9p1ouMyOb8GVVQNLfE1ttPBiHMy3M130_assertion description "[CSTB homozygous knockout mice show some parallels to the phenotype of human EPM1 including myoclonic seizures, development of ataxia and neuropathological changes associated with cell loss via apoptosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP415746.RAx4SlGc-vHiWaTB9p1ouMyOb8GVVQNLfE1ttPBiHMy3M130_provenance.
- NP415746.RAx4SlGc-vHiWaTB9p1ouMyOb8GVVQNLfE1ttPBiHMy3M130_assertion evidence source_evidence_literature NP415746.RAx4SlGc-vHiWaTB9p1ouMyOb8GVVQNLfE1ttPBiHMy3M130_provenance.
- NP415746.RAx4SlGc-vHiWaTB9p1ouMyOb8GVVQNLfE1ttPBiHMy3M130_assertion SIO_000772 14526183 NP415746.RAx4SlGc-vHiWaTB9p1ouMyOb8GVVQNLfE1ttPBiHMy3M130_provenance.
- NP415746.RAx4SlGc-vHiWaTB9p1ouMyOb8GVVQNLfE1ttPBiHMy3M130_assertion wasDerivedFrom befree-2016 NP415746.RAx4SlGc-vHiWaTB9p1ouMyOb8GVVQNLfE1ttPBiHMy3M130_provenance.
- NP415746.RAx4SlGc-vHiWaTB9p1ouMyOb8GVVQNLfE1ttPBiHMy3M130_assertion wasGeneratedBy ECO_0000203 NP415746.RAx4SlGc-vHiWaTB9p1ouMyOb8GVVQNLfE1ttPBiHMy3M130_provenance.
- befree-2016 importedOn "2016-02-19" NP415746.RAx4SlGc-vHiWaTB9p1ouMyOb8GVVQNLfE1ttPBiHMy3M130_provenance.