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- source_evidence_literature type ECO_0000212 NP882387.RA5VETN1ucdSBMGuyIp2ahtlopPYfbKz-8YVyUjQv6TwU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP882387.RA5VETN1ucdSBMGuyIp2ahtlopPYfbKz-8YVyUjQv6TwU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP882387.RA5VETN1ucdSBMGuyIp2ahtlopPYfbKz-8YVyUjQv6TwU130_provenance.
- NP882387.RA5VETN1ucdSBMGuyIp2ahtlopPYfbKz-8YVyUjQv6TwU130_assertion description "[To assess the possible association between the PTPN22 gene 1858C-->T polymorphism and the susceptibility to Henoch-Sch�nlein purpura (HSP) and determine if this polymorphism is implicated in the severity of this systemic vasculitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP882387.RA5VETN1ucdSBMGuyIp2ahtlopPYfbKz-8YVyUjQv6TwU130_provenance.
- NP882387.RA5VETN1ucdSBMGuyIp2ahtlopPYfbKz-8YVyUjQv6TwU130_assertion evidence source_evidence_literature NP882387.RA5VETN1ucdSBMGuyIp2ahtlopPYfbKz-8YVyUjQv6TwU130_provenance.
- NP882387.RA5VETN1ucdSBMGuyIp2ahtlopPYfbKz-8YVyUjQv6TwU130_assertion SIO_000772 18078626 NP882387.RA5VETN1ucdSBMGuyIp2ahtlopPYfbKz-8YVyUjQv6TwU130_provenance.
- NP882387.RA5VETN1ucdSBMGuyIp2ahtlopPYfbKz-8YVyUjQv6TwU130_assertion wasDerivedFrom befree-20150227 NP882387.RA5VETN1ucdSBMGuyIp2ahtlopPYfbKz-8YVyUjQv6TwU130_provenance.
- NP882387.RA5VETN1ucdSBMGuyIp2ahtlopPYfbKz-8YVyUjQv6TwU130_assertion wasGeneratedBy ECO_0000203 NP882387.RA5VETN1ucdSBMGuyIp2ahtlopPYfbKz-8YVyUjQv6TwU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP882387.RA5VETN1ucdSBMGuyIp2ahtlopPYfbKz-8YVyUjQv6TwU130_provenance.