Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP193673.RAjFpWEJ9xA8FujYSx-X4IUTQ86yNE6eGGQTJ9aU_B6Tc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP193673.RAjFpWEJ9xA8FujYSx-X4IUTQ86yNE6eGGQTJ9aU_B6Tc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP193673.RAjFpWEJ9xA8FujYSx-X4IUTQ86yNE6eGGQTJ9aU_B6Tc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP193673.RAjFpWEJ9xA8FujYSx-X4IUTQ86yNE6eGGQTJ9aU_B6Tc130_provenance.
- NP193673.RAjFpWEJ9xA8FujYSx-X4IUTQ86yNE6eGGQTJ9aU_B6Tc130_assertion description "[we observed a single nucleotide polymorphism (SNP) G351A leading to the silent mutation Gln117Gln.No significant difference was observed in the distribution of this GSTA4 polymorphism between Parkinson disease individuals and healthy controls]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP193673.RAjFpWEJ9xA8FujYSx-X4IUTQ86yNE6eGGQTJ9aU_B6Tc130_provenance.
- NP193673.RAjFpWEJ9xA8FujYSx-X4IUTQ86yNE6eGGQTJ9aU_B6Tc130_assertion evidence source_evidence_literature NP193673.RAjFpWEJ9xA8FujYSx-X4IUTQ86yNE6eGGQTJ9aU_B6Tc130_provenance.
- NP193673.RAjFpWEJ9xA8FujYSx-X4IUTQ86yNE6eGGQTJ9aU_B6Tc130_assertion SIO_000772 16054170 NP193673.RAjFpWEJ9xA8FujYSx-X4IUTQ86yNE6eGGQTJ9aU_B6Tc130_provenance.
- NP193673.RAjFpWEJ9xA8FujYSx-X4IUTQ86yNE6eGGQTJ9aU_B6Tc130_assertion wasDerivedFrom lhgdn-20090331 NP193673.RAjFpWEJ9xA8FujYSx-X4IUTQ86yNE6eGGQTJ9aU_B6Tc130_provenance.
- NP193673.RAjFpWEJ9xA8FujYSx-X4IUTQ86yNE6eGGQTJ9aU_B6Tc130_assertion wasGeneratedBy ECO_0000203 NP193673.RAjFpWEJ9xA8FujYSx-X4IUTQ86yNE6eGGQTJ9aU_B6Tc130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP193673.RAjFpWEJ9xA8FujYSx-X4IUTQ86yNE6eGGQTJ9aU_B6Tc130_provenance.