Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP201523.RAEXmKRuSGHMpNSxxfVdtVfEAzPdQe2sbddIsvW1XIoWw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP201523.RAEXmKRuSGHMpNSxxfVdtVfEAzPdQe2sbddIsvW1XIoWw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP201523.RAEXmKRuSGHMpNSxxfVdtVfEAzPdQe2sbddIsvW1XIoWw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP201523.RAEXmKRuSGHMpNSxxfVdtVfEAzPdQe2sbddIsvW1XIoWw130_provenance.
- NP201523.RAEXmKRuSGHMpNSxxfVdtVfEAzPdQe2sbddIsvW1XIoWw130_assertion description "[We previously described that a commonly occurring IRAK-1 variant haplotype, containing amino acid changes from serine to phenylalanine at position 196 and from leucine to serine at position 532, is associated with increased activation of NF-kappaB in LPS-stimulated neutrophils from patients with sepsis-induced acute lung injury and also higher mortality and more severe clinical outcomes in such patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP201523.RAEXmKRuSGHMpNSxxfVdtVfEAzPdQe2sbddIsvW1XIoWw130_provenance.
- NP201523.RAEXmKRuSGHMpNSxxfVdtVfEAzPdQe2sbddIsvW1XIoWw130_assertion evidence source_evidence_literature NP201523.RAEXmKRuSGHMpNSxxfVdtVfEAzPdQe2sbddIsvW1XIoWw130_provenance.
- NP201523.RAEXmKRuSGHMpNSxxfVdtVfEAzPdQe2sbddIsvW1XIoWw130_assertion SIO_000772 17785851 NP201523.RAEXmKRuSGHMpNSxxfVdtVfEAzPdQe2sbddIsvW1XIoWw130_provenance.
- NP201523.RAEXmKRuSGHMpNSxxfVdtVfEAzPdQe2sbddIsvW1XIoWw130_assertion wasDerivedFrom befree-20140225 NP201523.RAEXmKRuSGHMpNSxxfVdtVfEAzPdQe2sbddIsvW1XIoWw130_provenance.
- NP201523.RAEXmKRuSGHMpNSxxfVdtVfEAzPdQe2sbddIsvW1XIoWw130_assertion wasGeneratedBy ECO_0000203 NP201523.RAEXmKRuSGHMpNSxxfVdtVfEAzPdQe2sbddIsvW1XIoWw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP201523.RAEXmKRuSGHMpNSxxfVdtVfEAzPdQe2sbddIsvW1XIoWw130_provenance.