Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP974624.RAr51wWRHtVVfp1Xx_2pvMDU9KAlFmwlx51-iPI0YtU_s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP974624.RAr51wWRHtVVfp1Xx_2pvMDU9KAlFmwlx51-iPI0YtU_s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP974624.RAr51wWRHtVVfp1Xx_2pvMDU9KAlFmwlx51-iPI0YtU_s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP974624.RAr51wWRHtVVfp1Xx_2pvMDU9KAlFmwlx51-iPI0YtU_s130_provenance.
- NP974624.RAr51wWRHtVVfp1Xx_2pvMDU9KAlFmwlx51-iPI0YtU_s130_assertion description "[Mutations that truncate the C-terminal non-catalytic moiety of TTBK2 (tau tubulin kinase 2) cause the inherited, autosomal dominant, SCA11 (spinocerebellar ataxia type�11) movement disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP974624.RAr51wWRHtVVfp1Xx_2pvMDU9KAlFmwlx51-iPI0YtU_s130_provenance.
- NP974624.RAr51wWRHtVVfp1Xx_2pvMDU9KAlFmwlx51-iPI0YtU_s130_assertion evidence source_evidence_literature NP974624.RAr51wWRHtVVfp1Xx_2pvMDU9KAlFmwlx51-iPI0YtU_s130_provenance.
- NP974624.RAr51wWRHtVVfp1Xx_2pvMDU9KAlFmwlx51-iPI0YtU_s130_assertion SIO_000772 21548880 NP974624.RAr51wWRHtVVfp1Xx_2pvMDU9KAlFmwlx51-iPI0YtU_s130_provenance.
- NP974624.RAr51wWRHtVVfp1Xx_2pvMDU9KAlFmwlx51-iPI0YtU_s130_assertion wasDerivedFrom befree-20150227 NP974624.RAr51wWRHtVVfp1Xx_2pvMDU9KAlFmwlx51-iPI0YtU_s130_provenance.
- NP974624.RAr51wWRHtVVfp1Xx_2pvMDU9KAlFmwlx51-iPI0YtU_s130_assertion wasGeneratedBy ECO_0000203 NP974624.RAr51wWRHtVVfp1Xx_2pvMDU9KAlFmwlx51-iPI0YtU_s130_provenance.
- befree-20150227 importedOn "2015-02-27" NP974624.RAr51wWRHtVVfp1Xx_2pvMDU9KAlFmwlx51-iPI0YtU_s130_provenance.