Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP905404.RAW7VwTHg2tU4WjsqIcs8JmQFP5aGMacZNM2Lsf352tVM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP905404.RAW7VwTHg2tU4WjsqIcs8JmQFP5aGMacZNM2Lsf352tVM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP905404.RAW7VwTHg2tU4WjsqIcs8JmQFP5aGMacZNM2Lsf352tVM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP905404.RAW7VwTHg2tU4WjsqIcs8JmQFP5aGMacZNM2Lsf352tVM130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP905404.RAW7VwTHg2tU4WjsqIcs8JmQFP5aGMacZNM2Lsf352tVM130_provenance.