Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP905404.RAW7VwTHg2tU4WjsqIcs8JmQFP5aGMacZNM2Lsf352tVM130_assertion> ?p ?o ?g. }
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- NP905404.RAW7VwTHg2tU4WjsqIcs8JmQFP5aGMacZNM2Lsf352tVM130_assertion type Assertion NP905404.RAW7VwTHg2tU4WjsqIcs8JmQFP5aGMacZNM2Lsf352tVM130_head.
- NP905404.RAW7VwTHg2tU4WjsqIcs8JmQFP5aGMacZNM2Lsf352tVM130_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." NP905404.RAW7VwTHg2tU4WjsqIcs8JmQFP5aGMacZNM2Lsf352tVM130_provenance.
- NP905404.RAW7VwTHg2tU4WjsqIcs8JmQFP5aGMacZNM2Lsf352tVM130_assertion evidence source_evidence_literature NP905404.RAW7VwTHg2tU4WjsqIcs8JmQFP5aGMacZNM2Lsf352tVM130_provenance.
- NP905404.RAW7VwTHg2tU4WjsqIcs8JmQFP5aGMacZNM2Lsf352tVM130_assertion SIO_000772 8168815 NP905404.RAW7VwTHg2tU4WjsqIcs8JmQFP5aGMacZNM2Lsf352tVM130_provenance.
- NP905404.RAW7VwTHg2tU4WjsqIcs8JmQFP5aGMacZNM2Lsf352tVM130_assertion wasDerivedFrom befree-20140225 NP905404.RAW7VwTHg2tU4WjsqIcs8JmQFP5aGMacZNM2Lsf352tVM130_provenance.
- NP905404.RAW7VwTHg2tU4WjsqIcs8JmQFP5aGMacZNM2Lsf352tVM130_assertion wasGeneratedBy ECO_0000203 NP905404.RAW7VwTHg2tU4WjsqIcs8JmQFP5aGMacZNM2Lsf352tVM130_provenance.