Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP138639.RA0SghvetfyyVsE-2GxQXdzPAYM_IQpg36D1omiVIrtHc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP138639.RA0SghvetfyyVsE-2GxQXdzPAYM_IQpg36D1omiVIrtHc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP138639.RA0SghvetfyyVsE-2GxQXdzPAYM_IQpg36D1omiVIrtHc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP138639.RA0SghvetfyyVsE-2GxQXdzPAYM_IQpg36D1omiVIrtHc130_provenance.
- NP138639.RA0SghvetfyyVsE-2GxQXdzPAYM_IQpg36D1omiVIrtHc130_assertion description "[carriage of the GAA haplotype in FGB is associated with decreased mortality and less organ dysfunction in a cohort of critically ill patients with sepsis ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP138639.RA0SghvetfyyVsE-2GxQXdzPAYM_IQpg36D1omiVIrtHc130_provenance.
- NP138639.RA0SghvetfyyVsE-2GxQXdzPAYM_IQpg36D1omiVIrtHc130_assertion evidence source_evidence_literature NP138639.RA0SghvetfyyVsE-2GxQXdzPAYM_IQpg36D1omiVIrtHc130_provenance.
- NP138639.RA0SghvetfyyVsE-2GxQXdzPAYM_IQpg36D1omiVIrtHc130_assertion SIO_000772 17116333 NP138639.RA0SghvetfyyVsE-2GxQXdzPAYM_IQpg36D1omiVIrtHc130_provenance.
- NP138639.RA0SghvetfyyVsE-2GxQXdzPAYM_IQpg36D1omiVIrtHc130_assertion wasDerivedFrom lhgdn-20090331 NP138639.RA0SghvetfyyVsE-2GxQXdzPAYM_IQpg36D1omiVIrtHc130_provenance.
- NP138639.RA0SghvetfyyVsE-2GxQXdzPAYM_IQpg36D1omiVIrtHc130_assertion wasGeneratedBy ECO_0000203 NP138639.RA0SghvetfyyVsE-2GxQXdzPAYM_IQpg36D1omiVIrtHc130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP138639.RA0SghvetfyyVsE-2GxQXdzPAYM_IQpg36D1omiVIrtHc130_provenance.