Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP232190.RAkCucEqkeQ3Xl0SxKRXaFLXPEAJftc4hzjzoWRpHdBmM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP232190.RAkCucEqkeQ3Xl0SxKRXaFLXPEAJftc4hzjzoWRpHdBmM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP232190.RAkCucEqkeQ3Xl0SxKRXaFLXPEAJftc4hzjzoWRpHdBmM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP232190.RAkCucEqkeQ3Xl0SxKRXaFLXPEAJftc4hzjzoWRpHdBmM130_provenance.
- NP232190.RAkCucEqkeQ3Xl0SxKRXaFLXPEAJftc4hzjzoWRpHdBmM130_assertion description "[Results do not support a potential implication of the PTPN22 gene polymorphism in the susceptibility to and clinical expression of Henoch-Schonlein purpura.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP232190.RAkCucEqkeQ3Xl0SxKRXaFLXPEAJftc4hzjzoWRpHdBmM130_provenance.
- NP232190.RAkCucEqkeQ3Xl0SxKRXaFLXPEAJftc4hzjzoWRpHdBmM130_assertion evidence source_evidence_literature NP232190.RAkCucEqkeQ3Xl0SxKRXaFLXPEAJftc4hzjzoWRpHdBmM130_provenance.
- NP232190.RAkCucEqkeQ3Xl0SxKRXaFLXPEAJftc4hzjzoWRpHdBmM130_assertion SIO_000772 18078626 NP232190.RAkCucEqkeQ3Xl0SxKRXaFLXPEAJftc4hzjzoWRpHdBmM130_provenance.
- NP232190.RAkCucEqkeQ3Xl0SxKRXaFLXPEAJftc4hzjzoWRpHdBmM130_assertion wasDerivedFrom lhgdn-20090331 NP232190.RAkCucEqkeQ3Xl0SxKRXaFLXPEAJftc4hzjzoWRpHdBmM130_provenance.
- NP232190.RAkCucEqkeQ3Xl0SxKRXaFLXPEAJftc4hzjzoWRpHdBmM130_assertion wasGeneratedBy ECO_0000203 NP232190.RAkCucEqkeQ3Xl0SxKRXaFLXPEAJftc4hzjzoWRpHdBmM130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP232190.RAkCucEqkeQ3Xl0SxKRXaFLXPEAJftc4hzjzoWRpHdBmM130_provenance.