Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1334471.RA_S8WpsfCnjRiv4Bi2yhM2wPRu431S_1VZ004FB07L60130_assertion> ?p ?o ?g. }
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- NP1334471.RA_S8WpsfCnjRiv4Bi2yhM2wPRu431S_1VZ004FB07L60130_assertion type Assertion NP1334471.RA_S8WpsfCnjRiv4Bi2yhM2wPRu431S_1VZ004FB07L60130_head.
- NP1334471.RA_S8WpsfCnjRiv4Bi2yhM2wPRu431S_1VZ004FB07L60130_assertion description "[5%) of all chronic granulomatous disease (CGD) patients suffers from mutations in the gene encoding the small p22-phox subunit of the flavocytochrome b558 heterodimer, the terminal redox component of the phagocyte NADPH oxidase.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1334471.RA_S8WpsfCnjRiv4Bi2yhM2wPRu431S_1VZ004FB07L60130_provenance.
- NP1334471.RA_S8WpsfCnjRiv4Bi2yhM2wPRu431S_1VZ004FB07L60130_assertion evidence source_evidence_literature NP1334471.RA_S8WpsfCnjRiv4Bi2yhM2wPRu431S_1VZ004FB07L60130_provenance.
- NP1334471.RA_S8WpsfCnjRiv4Bi2yhM2wPRu431S_1VZ004FB07L60130_assertion SIO_000772 8168815 NP1334471.RA_S8WpsfCnjRiv4Bi2yhM2wPRu431S_1VZ004FB07L60130_provenance.
- NP1334471.RA_S8WpsfCnjRiv4Bi2yhM2wPRu431S_1VZ004FB07L60130_assertion wasDerivedFrom befree-2016 NP1334471.RA_S8WpsfCnjRiv4Bi2yhM2wPRu431S_1VZ004FB07L60130_provenance.
- NP1334471.RA_S8WpsfCnjRiv4Bi2yhM2wPRu431S_1VZ004FB07L60130_assertion wasGeneratedBy ECO_0000203 NP1334471.RA_S8WpsfCnjRiv4Bi2yhM2wPRu431S_1VZ004FB07L60130_provenance.