Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP343765.RAAHEijpM_POvSYRgsAvgGOy-GhoiSEnmEoLVStzAPv_o130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP343765.RAAHEijpM_POvSYRgsAvgGOy-GhoiSEnmEoLVStzAPv_o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP343765.RAAHEijpM_POvSYRgsAvgGOy-GhoiSEnmEoLVStzAPv_o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP343765.RAAHEijpM_POvSYRgsAvgGOy-GhoiSEnmEoLVStzAPv_o130_provenance.
- NP343765.RAAHEijpM_POvSYRgsAvgGOy-GhoiSEnmEoLVStzAPv_o130_assertion description "[Single nucleotide polymorphism (SNP) rs356165 is one of polymorphisms located in the 3'UTR and its association with PD has been reported but remains controversial.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP343765.RAAHEijpM_POvSYRgsAvgGOy-GhoiSEnmEoLVStzAPv_o130_provenance.
- NP343765.RAAHEijpM_POvSYRgsAvgGOy-GhoiSEnmEoLVStzAPv_o130_assertion evidence source_evidence_literature NP343765.RAAHEijpM_POvSYRgsAvgGOy-GhoiSEnmEoLVStzAPv_o130_provenance.
- NP343765.RAAHEijpM_POvSYRgsAvgGOy-GhoiSEnmEoLVStzAPv_o130_assertion SIO_000772 20478361 NP343765.RAAHEijpM_POvSYRgsAvgGOy-GhoiSEnmEoLVStzAPv_o130_provenance.
- NP343765.RAAHEijpM_POvSYRgsAvgGOy-GhoiSEnmEoLVStzAPv_o130_assertion wasDerivedFrom befree-20140225 NP343765.RAAHEijpM_POvSYRgsAvgGOy-GhoiSEnmEoLVStzAPv_o130_provenance.
- NP343765.RAAHEijpM_POvSYRgsAvgGOy-GhoiSEnmEoLVStzAPv_o130_assertion wasGeneratedBy ECO_0000203 NP343765.RAAHEijpM_POvSYRgsAvgGOy-GhoiSEnmEoLVStzAPv_o130_provenance.
- befree-20140225 importedOn "2014-02-25" NP343765.RAAHEijpM_POvSYRgsAvgGOy-GhoiSEnmEoLVStzAPv_o130_provenance.