Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP130499.RACpXrF2YGVkb4EL7BMSglsAfwo2fjzR0YrkWsw2OOi54130_assertion> ?p ?o ?g. }
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- NP130499.RACpXrF2YGVkb4EL7BMSglsAfwo2fjzR0YrkWsw2OOi54130_assertion type Assertion NP130499.RACpXrF2YGVkb4EL7BMSglsAfwo2fjzR0YrkWsw2OOi54130_head.
- NP130499.RACpXrF2YGVkb4EL7BMSglsAfwo2fjzR0YrkWsw2OOi54130_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." NP130499.RACpXrF2YGVkb4EL7BMSglsAfwo2fjzR0YrkWsw2OOi54130_provenance.
- NP130499.RACpXrF2YGVkb4EL7BMSglsAfwo2fjzR0YrkWsw2OOi54130_assertion evidence source_evidence_literature NP130499.RACpXrF2YGVkb4EL7BMSglsAfwo2fjzR0YrkWsw2OOi54130_provenance.
- NP130499.RACpXrF2YGVkb4EL7BMSglsAfwo2fjzR0YrkWsw2OOi54130_assertion SIO_000772 16054170 NP130499.RACpXrF2YGVkb4EL7BMSglsAfwo2fjzR0YrkWsw2OOi54130_provenance.
- NP130499.RACpXrF2YGVkb4EL7BMSglsAfwo2fjzR0YrkWsw2OOi54130_assertion wasDerivedFrom lhgdn-20090331 NP130499.RACpXrF2YGVkb4EL7BMSglsAfwo2fjzR0YrkWsw2OOi54130_provenance.
- NP130499.RACpXrF2YGVkb4EL7BMSglsAfwo2fjzR0YrkWsw2OOi54130_assertion wasGeneratedBy ECO_0000203 NP130499.RACpXrF2YGVkb4EL7BMSglsAfwo2fjzR0YrkWsw2OOi54130_provenance.