Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1099024.RA3DpLfNWXDkq5a7NvZ3lfWhgIbP3IYUCqAoCNhSHXHXs130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1099024.RA3DpLfNWXDkq5a7NvZ3lfWhgIbP3IYUCqAoCNhSHXHXs130_assertion type Assertion NP1099024.RA3DpLfNWXDkq5a7NvZ3lfWhgIbP3IYUCqAoCNhSHXHXs130_head.
- NP1099024.RA3DpLfNWXDkq5a7NvZ3lfWhgIbP3IYUCqAoCNhSHXHXs130_assertion description "[A mutation in one of the 4 genes encoding the components p22(phox), p47(phox), p67(phox), and p40(phox) of the leukocyte nicotinamide dinucleotide phosphate reduced (NADPH) oxidase leads to autosomal recessive (AR) CGD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1099024.RA3DpLfNWXDkq5a7NvZ3lfWhgIbP3IYUCqAoCNhSHXHXs130_provenance.
- NP1099024.RA3DpLfNWXDkq5a7NvZ3lfWhgIbP3IYUCqAoCNhSHXHXs130_assertion evidence source_evidence_literature NP1099024.RA3DpLfNWXDkq5a7NvZ3lfWhgIbP3IYUCqAoCNhSHXHXs130_provenance.
- NP1099024.RA3DpLfNWXDkq5a7NvZ3lfWhgIbP3IYUCqAoCNhSHXHXs130_assertion SIO_000772 23910690 NP1099024.RA3DpLfNWXDkq5a7NvZ3lfWhgIbP3IYUCqAoCNhSHXHXs130_provenance.
- NP1099024.RA3DpLfNWXDkq5a7NvZ3lfWhgIbP3IYUCqAoCNhSHXHXs130_assertion wasDerivedFrom befree-2016 NP1099024.RA3DpLfNWXDkq5a7NvZ3lfWhgIbP3IYUCqAoCNhSHXHXs130_provenance.
- NP1099024.RA3DpLfNWXDkq5a7NvZ3lfWhgIbP3IYUCqAoCNhSHXHXs130_assertion wasGeneratedBy ECO_0000203 NP1099024.RA3DpLfNWXDkq5a7NvZ3lfWhgIbP3IYUCqAoCNhSHXHXs130_provenance.