Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP585652.RA580kRr8PhyFVR1ILkaTmYutXwS0_NbNAlQla6wbQ9Ao130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP585652.RA580kRr8PhyFVR1ILkaTmYutXwS0_NbNAlQla6wbQ9Ao130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP585652.RA580kRr8PhyFVR1ILkaTmYutXwS0_NbNAlQla6wbQ9Ao130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP585652.RA580kRr8PhyFVR1ILkaTmYutXwS0_NbNAlQla6wbQ9Ao130_provenance.
- NP585652.RA580kRr8PhyFVR1ILkaTmYutXwS0_NbNAlQla6wbQ9Ao130_assertion description "[A mutation in one of the 4 genes encoding the components p22(phox), p47(phox), p67(phox), and p40(phox) of the leukocyte nicotinamide dinucleotide phosphate reduced (NADPH) oxidase leads to autosomal recessive (AR) CGD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP585652.RA580kRr8PhyFVR1ILkaTmYutXwS0_NbNAlQla6wbQ9Ao130_provenance.
- NP585652.RA580kRr8PhyFVR1ILkaTmYutXwS0_NbNAlQla6wbQ9Ao130_assertion evidence source_evidence_literature NP585652.RA580kRr8PhyFVR1ILkaTmYutXwS0_NbNAlQla6wbQ9Ao130_provenance.
- NP585652.RA580kRr8PhyFVR1ILkaTmYutXwS0_NbNAlQla6wbQ9Ao130_assertion SIO_000772 23910690 NP585652.RA580kRr8PhyFVR1ILkaTmYutXwS0_NbNAlQla6wbQ9Ao130_provenance.
- NP585652.RA580kRr8PhyFVR1ILkaTmYutXwS0_NbNAlQla6wbQ9Ao130_assertion wasDerivedFrom befree-20150227 NP585652.RA580kRr8PhyFVR1ILkaTmYutXwS0_NbNAlQla6wbQ9Ao130_provenance.
- NP585652.RA580kRr8PhyFVR1ILkaTmYutXwS0_NbNAlQla6wbQ9Ao130_assertion wasGeneratedBy ECO_0000203 NP585652.RA580kRr8PhyFVR1ILkaTmYutXwS0_NbNAlQla6wbQ9Ao130_provenance.
- befree-20150227 importedOn "2015-02-27" NP585652.RA580kRr8PhyFVR1ILkaTmYutXwS0_NbNAlQla6wbQ9Ao130_provenance.