Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP338932.RA3ioFK-nV4DpGUXWHHN7v78vDc9abSOvOoJxPbbKVuBk130_assertion> ?p ?o ?g. }
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- NP338932.RA3ioFK-nV4DpGUXWHHN7v78vDc9abSOvOoJxPbbKVuBk130_assertion type Assertion NP338932.RA3ioFK-nV4DpGUXWHHN7v78vDc9abSOvOoJxPbbKVuBk130_head.
- NP338932.RA3ioFK-nV4DpGUXWHHN7v78vDc9abSOvOoJxPbbKVuBk130_assertion description "[X-linked chronic granulomatous disease (X-CGD) is a primary immunodeficiency caused by mutations in the phagocyte nicotinamide dinucleotide phosphate oxidase catalytic subunit gp91(phox).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP338932.RA3ioFK-nV4DpGUXWHHN7v78vDc9abSOvOoJxPbbKVuBk130_provenance.
- NP338932.RA3ioFK-nV4DpGUXWHHN7v78vDc9abSOvOoJxPbbKVuBk130_assertion evidence source_evidence_literature NP338932.RA3ioFK-nV4DpGUXWHHN7v78vDc9abSOvOoJxPbbKVuBk130_provenance.
- NP338932.RA3ioFK-nV4DpGUXWHHN7v78vDc9abSOvOoJxPbbKVuBk130_assertion SIO_000772 17728796 NP338932.RA3ioFK-nV4DpGUXWHHN7v78vDc9abSOvOoJxPbbKVuBk130_provenance.
- NP338932.RA3ioFK-nV4DpGUXWHHN7v78vDc9abSOvOoJxPbbKVuBk130_assertion wasDerivedFrom befree-20150227 NP338932.RA3ioFK-nV4DpGUXWHHN7v78vDc9abSOvOoJxPbbKVuBk130_provenance.
- NP338932.RA3ioFK-nV4DpGUXWHHN7v78vDc9abSOvOoJxPbbKVuBk130_assertion wasGeneratedBy ECO_0000203 NP338932.RA3ioFK-nV4DpGUXWHHN7v78vDc9abSOvOoJxPbbKVuBk130_provenance.