Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP601312.RA17bZJbi1OQpQE6KB3XPkKEhNTqS7nAgfVXPEsgBFnZA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP601312.RA17bZJbi1OQpQE6KB3XPkKEhNTqS7nAgfVXPEsgBFnZA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP601312.RA17bZJbi1OQpQE6KB3XPkKEhNTqS7nAgfVXPEsgBFnZA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP601312.RA17bZJbi1OQpQE6KB3XPkKEhNTqS7nAgfVXPEsgBFnZA130_provenance.
- NP601312.RA17bZJbi1OQpQE6KB3XPkKEhNTqS7nAgfVXPEsgBFnZA130_assertion description "[Statistically significant differences in genotype, allele, and haplotype frequencies for 3 OAS2 single nucleotide polymorphisms (rs1293762, rs15895, and rs1732778) and 2 OAS3 single nucleotide polymorphisms (rs2285932 and rs2072136) were detected between patients with central nervous system disease and both those with fever and/or meningitis and the control group.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP601312.RA17bZJbi1OQpQE6KB3XPkKEhNTqS7nAgfVXPEsgBFnZA130_provenance.
- NP601312.RA17bZJbi1OQpQE6KB3XPkKEhNTqS7nAgfVXPEsgBFnZA130_assertion evidence source_evidence_literature NP601312.RA17bZJbi1OQpQE6KB3XPkKEhNTqS7nAgfVXPEsgBFnZA130_provenance.
- NP601312.RA17bZJbi1OQpQE6KB3XPkKEhNTqS7nAgfVXPEsgBFnZA130_assertion SIO_000772 21050126 NP601312.RA17bZJbi1OQpQE6KB3XPkKEhNTqS7nAgfVXPEsgBFnZA130_provenance.
- NP601312.RA17bZJbi1OQpQE6KB3XPkKEhNTqS7nAgfVXPEsgBFnZA130_assertion wasDerivedFrom befree-20150227 NP601312.RA17bZJbi1OQpQE6KB3XPkKEhNTqS7nAgfVXPEsgBFnZA130_provenance.
- NP601312.RA17bZJbi1OQpQE6KB3XPkKEhNTqS7nAgfVXPEsgBFnZA130_assertion wasGeneratedBy ECO_0000203 NP601312.RA17bZJbi1OQpQE6KB3XPkKEhNTqS7nAgfVXPEsgBFnZA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP601312.RA17bZJbi1OQpQE6KB3XPkKEhNTqS7nAgfVXPEsgBFnZA130_provenance.