Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP596110.RAsCPSy6ViG1Xtb2y8sdsUF5XC0n1GmCHHBcpaB4X2rb8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP596110.RAsCPSy6ViG1Xtb2y8sdsUF5XC0n1GmCHHBcpaB4X2rb8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP596110.RAsCPSy6ViG1Xtb2y8sdsUF5XC0n1GmCHHBcpaB4X2rb8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP596110.RAsCPSy6ViG1Xtb2y8sdsUF5XC0n1GmCHHBcpaB4X2rb8130_provenance.
- NP596110.RAsCPSy6ViG1Xtb2y8sdsUF5XC0n1GmCHHBcpaB4X2rb8130_assertion description "[Genetic testing in spinocerebellar ataxia in Taiwan: expansions of trinucleotide repeats in SCA8 and SCA17 are associated with typical Parkinson's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP596110.RAsCPSy6ViG1Xtb2y8sdsUF5XC0n1GmCHHBcpaB4X2rb8130_provenance.
- NP596110.RAsCPSy6ViG1Xtb2y8sdsUF5XC0n1GmCHHBcpaB4X2rb8130_assertion evidence source_evidence_literature NP596110.RAsCPSy6ViG1Xtb2y8sdsUF5XC0n1GmCHHBcpaB4X2rb8130_provenance.
- NP596110.RAsCPSy6ViG1Xtb2y8sdsUF5XC0n1GmCHHBcpaB4X2rb8130_assertion SIO_000772 14756671 NP596110.RAsCPSy6ViG1Xtb2y8sdsUF5XC0n1GmCHHBcpaB4X2rb8130_provenance.
- NP596110.RAsCPSy6ViG1Xtb2y8sdsUF5XC0n1GmCHHBcpaB4X2rb8130_assertion wasDerivedFrom befree-20140225 NP596110.RAsCPSy6ViG1Xtb2y8sdsUF5XC0n1GmCHHBcpaB4X2rb8130_provenance.
- NP596110.RAsCPSy6ViG1Xtb2y8sdsUF5XC0n1GmCHHBcpaB4X2rb8130_assertion wasGeneratedBy ECO_0000203 NP596110.RAsCPSy6ViG1Xtb2y8sdsUF5XC0n1GmCHHBcpaB4X2rb8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP596110.RAsCPSy6ViG1Xtb2y8sdsUF5XC0n1GmCHHBcpaB4X2rb8130_provenance.