Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP280590.RAa63CuItvn6JRanKLp2SHavaZRZvntzPvoXmNO6IcSLE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP280590.RAa63CuItvn6JRanKLp2SHavaZRZvntzPvoXmNO6IcSLE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP280590.RAa63CuItvn6JRanKLp2SHavaZRZvntzPvoXmNO6IcSLE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP280590.RAa63CuItvn6JRanKLp2SHavaZRZvntzPvoXmNO6IcSLE130_provenance.
- NP280590.RAa63CuItvn6JRanKLp2SHavaZRZvntzPvoXmNO6IcSLE130_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." NP280590.RAa63CuItvn6JRanKLp2SHavaZRZvntzPvoXmNO6IcSLE130_provenance.
- NP280590.RAa63CuItvn6JRanKLp2SHavaZRZvntzPvoXmNO6IcSLE130_assertion evidence source_evidence_literature NP280590.RAa63CuItvn6JRanKLp2SHavaZRZvntzPvoXmNO6IcSLE130_provenance.
- NP280590.RAa63CuItvn6JRanKLp2SHavaZRZvntzPvoXmNO6IcSLE130_assertion SIO_000772 18078626 NP280590.RAa63CuItvn6JRanKLp2SHavaZRZvntzPvoXmNO6IcSLE130_provenance.
- NP280590.RAa63CuItvn6JRanKLp2SHavaZRZvntzPvoXmNO6IcSLE130_assertion wasDerivedFrom befree-20140225 NP280590.RAa63CuItvn6JRanKLp2SHavaZRZvntzPvoXmNO6IcSLE130_provenance.
- NP280590.RAa63CuItvn6JRanKLp2SHavaZRZvntzPvoXmNO6IcSLE130_assertion wasGeneratedBy ECO_0000203 NP280590.RAa63CuItvn6JRanKLp2SHavaZRZvntzPvoXmNO6IcSLE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP280590.RAa63CuItvn6JRanKLp2SHavaZRZvntzPvoXmNO6IcSLE130_provenance.