Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP214930.RAKS6x1d1Vb44Ss8bAQQcFVLJdrejGL_ONeIE6kTlEHow130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP214930.RAKS6x1d1Vb44Ss8bAQQcFVLJdrejGL_ONeIE6kTlEHow130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP214930.RAKS6x1d1Vb44Ss8bAQQcFVLJdrejGL_ONeIE6kTlEHow130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP214930.RAKS6x1d1Vb44Ss8bAQQcFVLJdrejGL_ONeIE6kTlEHow130_provenance.
- NP214930.RAKS6x1d1Vb44Ss8bAQQcFVLJdrejGL_ONeIE6kTlEHow130_assertion description "[Our data indicate that a common variant of the CD18 gene confers increased risk for CSS and MP, supporting that genetic factors are involved in the etiology and pathogenesis of ANCA-associated systemic vasculitides.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP214930.RAKS6x1d1Vb44Ss8bAQQcFVLJdrejGL_ONeIE6kTlEHow130_provenance.
- NP214930.RAKS6x1d1Vb44Ss8bAQQcFVLJdrejGL_ONeIE6kTlEHow130_assertion evidence source_evidence_literature NP214930.RAKS6x1d1Vb44Ss8bAQQcFVLJdrejGL_ONeIE6kTlEHow130_provenance.
- NP214930.RAKS6x1d1Vb44Ss8bAQQcFVLJdrejGL_ONeIE6kTlEHow130_assertion SIO_000772 10607485 NP214930.RAKS6x1d1Vb44Ss8bAQQcFVLJdrejGL_ONeIE6kTlEHow130_provenance.
- NP214930.RAKS6x1d1Vb44Ss8bAQQcFVLJdrejGL_ONeIE6kTlEHow130_assertion wasDerivedFrom befree-20140225 NP214930.RAKS6x1d1Vb44Ss8bAQQcFVLJdrejGL_ONeIE6kTlEHow130_provenance.
- NP214930.RAKS6x1d1Vb44Ss8bAQQcFVLJdrejGL_ONeIE6kTlEHow130_assertion wasGeneratedBy ECO_0000203 NP214930.RAKS6x1d1Vb44Ss8bAQQcFVLJdrejGL_ONeIE6kTlEHow130_provenance.
- befree-20140225 importedOn "2014-02-25" NP214930.RAKS6x1d1Vb44Ss8bAQQcFVLJdrejGL_ONeIE6kTlEHow130_provenance.