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- source_evidence_literature type ECO_0000212 NP338803.RA881E65z8MiSK-tsIiGY2QkTlBSowNsAXBw-mdudWIO4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP338803.RA881E65z8MiSK-tsIiGY2QkTlBSowNsAXBw-mdudWIO4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP338803.RA881E65z8MiSK-tsIiGY2QkTlBSowNsAXBw-mdudWIO4130_provenance.
- NP338803.RA881E65z8MiSK-tsIiGY2QkTlBSowNsAXBw-mdudWIO4130_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." NP338803.RA881E65z8MiSK-tsIiGY2QkTlBSowNsAXBw-mdudWIO4130_provenance.
- NP338803.RA881E65z8MiSK-tsIiGY2QkTlBSowNsAXBw-mdudWIO4130_assertion evidence source_evidence_literature NP338803.RA881E65z8MiSK-tsIiGY2QkTlBSowNsAXBw-mdudWIO4130_provenance.
- NP338803.RA881E65z8MiSK-tsIiGY2QkTlBSowNsAXBw-mdudWIO4130_assertion SIO_000772 8168815 NP338803.RA881E65z8MiSK-tsIiGY2QkTlBSowNsAXBw-mdudWIO4130_provenance.
- NP338803.RA881E65z8MiSK-tsIiGY2QkTlBSowNsAXBw-mdudWIO4130_assertion wasDerivedFrom befree-20150227 NP338803.RA881E65z8MiSK-tsIiGY2QkTlBSowNsAXBw-mdudWIO4130_provenance.
- NP338803.RA881E65z8MiSK-tsIiGY2QkTlBSowNsAXBw-mdudWIO4130_assertion wasGeneratedBy ECO_0000203 NP338803.RA881E65z8MiSK-tsIiGY2QkTlBSowNsAXBw-mdudWIO4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP338803.RA881E65z8MiSK-tsIiGY2QkTlBSowNsAXBw-mdudWIO4130_provenance.