Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP541150.RACTPHN23pYU1Q0H0sMaVmDfPqUcL2TdOHx5AGliqD62g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP541150.RACTPHN23pYU1Q0H0sMaVmDfPqUcL2TdOHx5AGliqD62g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP541150.RACTPHN23pYU1Q0H0sMaVmDfPqUcL2TdOHx5AGliqD62g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP541150.RACTPHN23pYU1Q0H0sMaVmDfPqUcL2TdOHx5AGliqD62g130_provenance.
- NP541150.RACTPHN23pYU1Q0H0sMaVmDfPqUcL2TdOHx5AGliqD62g130_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." NP541150.RACTPHN23pYU1Q0H0sMaVmDfPqUcL2TdOHx5AGliqD62g130_provenance.
- NP541150.RACTPHN23pYU1Q0H0sMaVmDfPqUcL2TdOHx5AGliqD62g130_assertion evidence source_evidence_literature NP541150.RACTPHN23pYU1Q0H0sMaVmDfPqUcL2TdOHx5AGliqD62g130_provenance.
- NP541150.RACTPHN23pYU1Q0H0sMaVmDfPqUcL2TdOHx5AGliqD62g130_assertion SIO_000772 10607485 NP541150.RACTPHN23pYU1Q0H0sMaVmDfPqUcL2TdOHx5AGliqD62g130_provenance.
- NP541150.RACTPHN23pYU1Q0H0sMaVmDfPqUcL2TdOHx5AGliqD62g130_assertion wasDerivedFrom befree-20150227 NP541150.RACTPHN23pYU1Q0H0sMaVmDfPqUcL2TdOHx5AGliqD62g130_provenance.
- NP541150.RACTPHN23pYU1Q0H0sMaVmDfPqUcL2TdOHx5AGliqD62g130_assertion wasGeneratedBy ECO_0000203 NP541150.RACTPHN23pYU1Q0H0sMaVmDfPqUcL2TdOHx5AGliqD62g130_provenance.
- befree-20150227 importedOn "2015-02-27" NP541150.RACTPHN23pYU1Q0H0sMaVmDfPqUcL2TdOHx5AGliqD62g130_provenance.