Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP645084.RAYC3xvsiPtRgZyHxGnzWIRkXGLlxf3BkNvOIv7x1UzVw130_assertion> ?p ?o ?g. }
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- NP645084.RAYC3xvsiPtRgZyHxGnzWIRkXGLlxf3BkNvOIv7x1UzVw130_assertion type Assertion NP645084.RAYC3xvsiPtRgZyHxGnzWIRkXGLlxf3BkNvOIv7x1UzVw130_head.
- NP645084.RAYC3xvsiPtRgZyHxGnzWIRkXGLlxf3BkNvOIv7x1UzVw130_assertion description "[Lack of association of a functional single nucleotide polymorphism of PTPN22, encoding lymphoid protein phosphatase, with susceptibility to Henoch-Sch�nlein purpura.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP645084.RAYC3xvsiPtRgZyHxGnzWIRkXGLlxf3BkNvOIv7x1UzVw130_provenance.
- NP645084.RAYC3xvsiPtRgZyHxGnzWIRkXGLlxf3BkNvOIv7x1UzVw130_assertion evidence source_evidence_literature NP645084.RAYC3xvsiPtRgZyHxGnzWIRkXGLlxf3BkNvOIv7x1UzVw130_provenance.
- NP645084.RAYC3xvsiPtRgZyHxGnzWIRkXGLlxf3BkNvOIv7x1UzVw130_assertion SIO_000772 18078626 NP645084.RAYC3xvsiPtRgZyHxGnzWIRkXGLlxf3BkNvOIv7x1UzVw130_provenance.
- NP645084.RAYC3xvsiPtRgZyHxGnzWIRkXGLlxf3BkNvOIv7x1UzVw130_assertion wasDerivedFrom befree-2016 NP645084.RAYC3xvsiPtRgZyHxGnzWIRkXGLlxf3BkNvOIv7x1UzVw130_provenance.
- NP645084.RAYC3xvsiPtRgZyHxGnzWIRkXGLlxf3BkNvOIv7x1UzVw130_assertion wasGeneratedBy ECO_0000203 NP645084.RAYC3xvsiPtRgZyHxGnzWIRkXGLlxf3BkNvOIv7x1UzVw130_provenance.