Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1091399.RA8vIWM7gjTF107W5aHyE0TNXTnMC2DjYGifAMkLDrCa0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1091399.RA8vIWM7gjTF107W5aHyE0TNXTnMC2DjYGifAMkLDrCa0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1091399.RA8vIWM7gjTF107W5aHyE0TNXTnMC2DjYGifAMkLDrCa0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1091399.RA8vIWM7gjTF107W5aHyE0TNXTnMC2DjYGifAMkLDrCa0130_provenance.
- befree-2016 importedOn "2016-02-19" NP1091399.RA8vIWM7gjTF107W5aHyE0TNXTnMC2DjYGifAMkLDrCa0130_provenance.
- NP1091399.RA8vIWM7gjTF107W5aHyE0TNXTnMC2DjYGifAMkLDrCa0130_assertion wasGeneratedBy ECO_0000203 NP1091399.RA8vIWM7gjTF107W5aHyE0TNXTnMC2DjYGifAMkLDrCa0130_provenance.
- NP1091399.RA8vIWM7gjTF107W5aHyE0TNXTnMC2DjYGifAMkLDrCa0130_assertion wasDerivedFrom befree-2016 NP1091399.RA8vIWM7gjTF107W5aHyE0TNXTnMC2DjYGifAMkLDrCa0130_provenance.
- NP1091399.RA8vIWM7gjTF107W5aHyE0TNXTnMC2DjYGifAMkLDrCa0130_assertion SIO_000772 23826567 NP1091399.RA8vIWM7gjTF107W5aHyE0TNXTnMC2DjYGifAMkLDrCa0130_provenance.
- NP1091399.RA8vIWM7gjTF107W5aHyE0TNXTnMC2DjYGifAMkLDrCa0130_assertion evidence source_evidence_literature NP1091399.RA8vIWM7gjTF107W5aHyE0TNXTnMC2DjYGifAMkLDrCa0130_provenance.
- NP1091399.RA8vIWM7gjTF107W5aHyE0TNXTnMC2DjYGifAMkLDrCa0130_assertion description "[Chronic granulomatous disease (CGD) is a rare genetic disease, which is caused by defects in the NADPH oxidase complex (gp91(phox), p22(phox), p40(phox), p47(phox), and p67(phox)) of phagocytes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1091399.RA8vIWM7gjTF107W5aHyE0TNXTnMC2DjYGifAMkLDrCa0130_provenance.