Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP584866.RA0nmV59yg_zwHWZ-sTtqhWZtnGKe7IM1oDNEC8qTvPTw130_assertion> ?p ?o ?g. }
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- NP584866.RA0nmV59yg_zwHWZ-sTtqhWZtnGKe7IM1oDNEC8qTvPTw130_assertion type Assertion NP584866.RA0nmV59yg_zwHWZ-sTtqhWZtnGKe7IM1oDNEC8qTvPTw130_head.
- NP584866.RA0nmV59yg_zwHWZ-sTtqhWZtnGKe7IM1oDNEC8qTvPTw130_assertion description "[Gp91phox is encoded on the X-chromosome and p22phox, p47phox and p67phox on different autosomal chromosomes, and a defect in one of these components leads to CGD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP584866.RA0nmV59yg_zwHWZ-sTtqhWZtnGKe7IM1oDNEC8qTvPTw130_provenance.
- NP584866.RA0nmV59yg_zwHWZ-sTtqhWZtnGKe7IM1oDNEC8qTvPTw130_assertion evidence source_evidence_literature NP584866.RA0nmV59yg_zwHWZ-sTtqhWZtnGKe7IM1oDNEC8qTvPTw130_provenance.
- NP584866.RA0nmV59yg_zwHWZ-sTtqhWZtnGKe7IM1oDNEC8qTvPTw130_assertion SIO_000772 9618766 NP584866.RA0nmV59yg_zwHWZ-sTtqhWZtnGKe7IM1oDNEC8qTvPTw130_provenance.
- NP584866.RA0nmV59yg_zwHWZ-sTtqhWZtnGKe7IM1oDNEC8qTvPTw130_assertion wasDerivedFrom befree-20140225 NP584866.RA0nmV59yg_zwHWZ-sTtqhWZtnGKe7IM1oDNEC8qTvPTw130_provenance.
- NP584866.RA0nmV59yg_zwHWZ-sTtqhWZtnGKe7IM1oDNEC8qTvPTw130_assertion wasGeneratedBy ECO_0000203 NP584866.RA0nmV59yg_zwHWZ-sTtqhWZtnGKe7IM1oDNEC8qTvPTw130_provenance.