Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP208373.RA4Tsz_LqOrksL7FosHu0UTQSoSq4Ddee8hHJxTSfawyc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP208373.RA4Tsz_LqOrksL7FosHu0UTQSoSq4Ddee8hHJxTSfawyc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP208373.RA4Tsz_LqOrksL7FosHu0UTQSoSq4Ddee8hHJxTSfawyc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP208373.RA4Tsz_LqOrksL7FosHu0UTQSoSq4Ddee8hHJxTSfawyc130_provenance.
- NP208373.RA4Tsz_LqOrksL7FosHu0UTQSoSq4Ddee8hHJxTSfawyc130_assertion description "[Variant MBL2 structural genotype constitutes a significant risk factor for reactive amyloidosis in RA and that the increased risk is probably related to MBL-mediated impairment of mononuclear phagocyte function.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP208373.RA4Tsz_LqOrksL7FosHu0UTQSoSq4Ddee8hHJxTSfawyc130_provenance.
- NP208373.RA4Tsz_LqOrksL7FosHu0UTQSoSq4Ddee8hHJxTSfawyc130_assertion evidence source_evidence_literature NP208373.RA4Tsz_LqOrksL7FosHu0UTQSoSq4Ddee8hHJxTSfawyc130_provenance.
- NP208373.RA4Tsz_LqOrksL7FosHu0UTQSoSq4Ddee8hHJxTSfawyc130_assertion SIO_000772 17875183 NP208373.RA4Tsz_LqOrksL7FosHu0UTQSoSq4Ddee8hHJxTSfawyc130_provenance.
- NP208373.RA4Tsz_LqOrksL7FosHu0UTQSoSq4Ddee8hHJxTSfawyc130_assertion wasDerivedFrom lhgdn-20090331 NP208373.RA4Tsz_LqOrksL7FosHu0UTQSoSq4Ddee8hHJxTSfawyc130_provenance.
- NP208373.RA4Tsz_LqOrksL7FosHu0UTQSoSq4Ddee8hHJxTSfawyc130_assertion wasGeneratedBy ECO_0000203 NP208373.RA4Tsz_LqOrksL7FosHu0UTQSoSq4Ddee8hHJxTSfawyc130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP208373.RA4Tsz_LqOrksL7FosHu0UTQSoSq4Ddee8hHJxTSfawyc130_provenance.