Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP682291.RAXA_KQ0DU06FLs1WsP_mZjNs6xniqgOvCiTvttuAwkmU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP682291.RAXA_KQ0DU06FLs1WsP_mZjNs6xniqgOvCiTvttuAwkmU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP682291.RAXA_KQ0DU06FLs1WsP_mZjNs6xniqgOvCiTvttuAwkmU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP682291.RAXA_KQ0DU06FLs1WsP_mZjNs6xniqgOvCiTvttuAwkmU130_provenance.
- NP682291.RAXA_KQ0DU06FLs1WsP_mZjNs6xniqgOvCiTvttuAwkmU130_assertion description "[These results show that the loss of Atp13a2 causes sensorimotor impairments, ?-synuclein accumulation as occurs in PD and related synucleinopathies, and accumulation of lipofuscin deposits characteristic of NCL, thus providing the first direct demonstration that null mutations in Atp13a2 can cause pathological features of both diseases in the same organism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP682291.RAXA_KQ0DU06FLs1WsP_mZjNs6xniqgOvCiTvttuAwkmU130_provenance.
- NP682291.RAXA_KQ0DU06FLs1WsP_mZjNs6xniqgOvCiTvttuAwkmU130_assertion evidence source_evidence_literature NP682291.RAXA_KQ0DU06FLs1WsP_mZjNs6xniqgOvCiTvttuAwkmU130_provenance.
- NP682291.RAXA_KQ0DU06FLs1WsP_mZjNs6xniqgOvCiTvttuAwkmU130_assertion SIO_000772 23393156 NP682291.RAXA_KQ0DU06FLs1WsP_mZjNs6xniqgOvCiTvttuAwkmU130_provenance.
- NP682291.RAXA_KQ0DU06FLs1WsP_mZjNs6xniqgOvCiTvttuAwkmU130_assertion wasDerivedFrom befree-20140225 NP682291.RAXA_KQ0DU06FLs1WsP_mZjNs6xniqgOvCiTvttuAwkmU130_provenance.
- NP682291.RAXA_KQ0DU06FLs1WsP_mZjNs6xniqgOvCiTvttuAwkmU130_assertion wasGeneratedBy ECO_0000203 NP682291.RAXA_KQ0DU06FLs1WsP_mZjNs6xniqgOvCiTvttuAwkmU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP682291.RAXA_KQ0DU06FLs1WsP_mZjNs6xniqgOvCiTvttuAwkmU130_provenance.