Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP795057.RAw8HhgxsxMip_gxOiPVNQW1aNLVylPRpjQJA0ShBgBYI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP795057.RAw8HhgxsxMip_gxOiPVNQW1aNLVylPRpjQJA0ShBgBYI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP795057.RAw8HhgxsxMip_gxOiPVNQW1aNLVylPRpjQJA0ShBgBYI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP795057.RAw8HhgxsxMip_gxOiPVNQW1aNLVylPRpjQJA0ShBgBYI130_provenance.
- NP795057.RAw8HhgxsxMip_gxOiPVNQW1aNLVylPRpjQJA0ShBgBYI130_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." NP795057.RAw8HhgxsxMip_gxOiPVNQW1aNLVylPRpjQJA0ShBgBYI130_provenance.
- NP795057.RAw8HhgxsxMip_gxOiPVNQW1aNLVylPRpjQJA0ShBgBYI130_assertion evidence source_evidence_literature NP795057.RAw8HhgxsxMip_gxOiPVNQW1aNLVylPRpjQJA0ShBgBYI130_provenance.
- NP795057.RAw8HhgxsxMip_gxOiPVNQW1aNLVylPRpjQJA0ShBgBYI130_assertion SIO_000772 21548880 NP795057.RAw8HhgxsxMip_gxOiPVNQW1aNLVylPRpjQJA0ShBgBYI130_provenance.
- NP795057.RAw8HhgxsxMip_gxOiPVNQW1aNLVylPRpjQJA0ShBgBYI130_assertion wasDerivedFrom befree-20140225 NP795057.RAw8HhgxsxMip_gxOiPVNQW1aNLVylPRpjQJA0ShBgBYI130_provenance.
- NP795057.RAw8HhgxsxMip_gxOiPVNQW1aNLVylPRpjQJA0ShBgBYI130_assertion wasGeneratedBy ECO_0000203 NP795057.RAw8HhgxsxMip_gxOiPVNQW1aNLVylPRpjQJA0ShBgBYI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP795057.RAw8HhgxsxMip_gxOiPVNQW1aNLVylPRpjQJA0ShBgBYI130_provenance.