Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1334882.RALR1DU5AhF6o76r8wDRy6LFOyGh_nOOlOvs07b5flotU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1334882.RALR1DU5AhF6o76r8wDRy6LFOyGh_nOOlOvs07b5flotU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1334882.RALR1DU5AhF6o76r8wDRy6LFOyGh_nOOlOvs07b5flotU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1334882.RALR1DU5AhF6o76r8wDRy6LFOyGh_nOOlOvs07b5flotU130_provenance.
- NP1334882.RALR1DU5AhF6o76r8wDRy6LFOyGh_nOOlOvs07b5flotU130_assertion description "[Patients suffering from chronic granulomatous disease (CGD) are defective in one of the following components: p47-phox and p67-phox, residing in the cytosol of resting phagocytes, and gp91-phox and p22-phox, constituting the membrane-bound cytochrome b558.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1334882.RALR1DU5AhF6o76r8wDRy6LFOyGh_nOOlOvs07b5flotU130_provenance.
- NP1334882.RALR1DU5AhF6o76r8wDRy6LFOyGh_nOOlOvs07b5flotU130_assertion evidence source_evidence_literature NP1334882.RALR1DU5AhF6o76r8wDRy6LFOyGh_nOOlOvs07b5flotU130_provenance.
- NP1334882.RALR1DU5AhF6o76r8wDRy6LFOyGh_nOOlOvs07b5flotU130_assertion SIO_000772 8182143 NP1334882.RALR1DU5AhF6o76r8wDRy6LFOyGh_nOOlOvs07b5flotU130_provenance.
- NP1334882.RALR1DU5AhF6o76r8wDRy6LFOyGh_nOOlOvs07b5flotU130_assertion wasDerivedFrom befree-2016 NP1334882.RALR1DU5AhF6o76r8wDRy6LFOyGh_nOOlOvs07b5flotU130_provenance.
- NP1334882.RALR1DU5AhF6o76r8wDRy6LFOyGh_nOOlOvs07b5flotU130_assertion wasGeneratedBy ECO_0000203 NP1334882.RALR1DU5AhF6o76r8wDRy6LFOyGh_nOOlOvs07b5flotU130_provenance.
- befree-2016 importedOn "2016-02-19" NP1334882.RALR1DU5AhF6o76r8wDRy6LFOyGh_nOOlOvs07b5flotU130_provenance.