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- source_evidence_literature type ECO_0000212 NP645084.RAYC3xvsiPtRgZyHxGnzWIRkXGLlxf3BkNvOIv7x1UzVw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP645084.RAYC3xvsiPtRgZyHxGnzWIRkXGLlxf3BkNvOIv7x1UzVw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP645084.RAYC3xvsiPtRgZyHxGnzWIRkXGLlxf3BkNvOIv7x1UzVw130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP645084.RAYC3xvsiPtRgZyHxGnzWIRkXGLlxf3BkNvOIv7x1UzVw130_provenance.