Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP406512.RAOw7765FzAqnSOCM5PKXK_898YG-kFFOagce79I1X2jY130_assertion> ?p ?o ?g. }
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- NP406512.RAOw7765FzAqnSOCM5PKXK_898YG-kFFOagce79I1X2jY130_assertion type Assertion NP406512.RAOw7765FzAqnSOCM5PKXK_898YG-kFFOagce79I1X2jY130_head.
- NP406512.RAOw7765FzAqnSOCM5PKXK_898YG-kFFOagce79I1X2jY130_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." NP406512.RAOw7765FzAqnSOCM5PKXK_898YG-kFFOagce79I1X2jY130_provenance.
- NP406512.RAOw7765FzAqnSOCM5PKXK_898YG-kFFOagce79I1X2jY130_assertion evidence source_evidence_literature NP406512.RAOw7765FzAqnSOCM5PKXK_898YG-kFFOagce79I1X2jY130_provenance.
- NP406512.RAOw7765FzAqnSOCM5PKXK_898YG-kFFOagce79I1X2jY130_assertion SIO_000772 8168815 NP406512.RAOw7765FzAqnSOCM5PKXK_898YG-kFFOagce79I1X2jY130_provenance.
- NP406512.RAOw7765FzAqnSOCM5PKXK_898YG-kFFOagce79I1X2jY130_assertion wasDerivedFrom befree-20140225 NP406512.RAOw7765FzAqnSOCM5PKXK_898YG-kFFOagce79I1X2jY130_provenance.
- NP406512.RAOw7765FzAqnSOCM5PKXK_898YG-kFFOagce79I1X2jY130_assertion wasGeneratedBy ECO_0000203 NP406512.RAOw7765FzAqnSOCM5PKXK_898YG-kFFOagce79I1X2jY130_provenance.