Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1222019.RAf2KtNZBWO2usuzBadsLX7TKoyg5NA93_YEtxQUqwUpc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1222019.RAf2KtNZBWO2usuzBadsLX7TKoyg5NA93_YEtxQUqwUpc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1222019.RAf2KtNZBWO2usuzBadsLX7TKoyg5NA93_YEtxQUqwUpc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1222019.RAf2KtNZBWO2usuzBadsLX7TKoyg5NA93_YEtxQUqwUpc130_provenance.
- NP1222019.RAf2KtNZBWO2usuzBadsLX7TKoyg5NA93_YEtxQUqwUpc130_assertion description "[This difference was comparable in p47(phox)- and gp91(phox)-deficient subtypes of CGD and independent of risk factors in multivariate regression analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1222019.RAf2KtNZBWO2usuzBadsLX7TKoyg5NA93_YEtxQUqwUpc130_provenance.
- NP1222019.RAf2KtNZBWO2usuzBadsLX7TKoyg5NA93_YEtxQUqwUpc130_assertion evidence source_evidence_literature NP1222019.RAf2KtNZBWO2usuzBadsLX7TKoyg5NA93_YEtxQUqwUpc130_provenance.
- NP1222019.RAf2KtNZBWO2usuzBadsLX7TKoyg5NA93_YEtxQUqwUpc130_assertion SIO_000772 25239440 NP1222019.RAf2KtNZBWO2usuzBadsLX7TKoyg5NA93_YEtxQUqwUpc130_provenance.
- NP1222019.RAf2KtNZBWO2usuzBadsLX7TKoyg5NA93_YEtxQUqwUpc130_assertion wasDerivedFrom befree-2016 NP1222019.RAf2KtNZBWO2usuzBadsLX7TKoyg5NA93_YEtxQUqwUpc130_provenance.
- NP1222019.RAf2KtNZBWO2usuzBadsLX7TKoyg5NA93_YEtxQUqwUpc130_assertion wasGeneratedBy ECO_0000203 NP1222019.RAf2KtNZBWO2usuzBadsLX7TKoyg5NA93_YEtxQUqwUpc130_provenance.
- befree-2016 importedOn "2016-02-19" NP1222019.RAf2KtNZBWO2usuzBadsLX7TKoyg5NA93_YEtxQUqwUpc130_provenance.