Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP232190.RAkCucEqkeQ3Xl0SxKRXaFLXPEAJftc4hzjzoWRpHdBmM130_assertion> ?p ?o ?g. }
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- NP232190.RAkCucEqkeQ3Xl0SxKRXaFLXPEAJftc4hzjzoWRpHdBmM130_assertion type Assertion NP232190.RAkCucEqkeQ3Xl0SxKRXaFLXPEAJftc4hzjzoWRpHdBmM130_head.
- 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.