Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP203056.RAa-dsL6p1dCNvGYGGIqUUMYSb3o7EJlvkPmCvb-a9BAA130_assertion> ?p ?o ?g. }
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- NP203056.RAa-dsL6p1dCNvGYGGIqUUMYSb3o7EJlvkPmCvb-a9BAA130_assertion type Assertion NP203056.RAa-dsL6p1dCNvGYGGIqUUMYSb3o7EJlvkPmCvb-a9BAA130_head.
- NP203056.RAa-dsL6p1dCNvGYGGIqUUMYSb3o7EJlvkPmCvb-a9BAA130_assertion wasGeneratedBy ECO_0000203 NP203056.RAa-dsL6p1dCNvGYGGIqUUMYSb3o7EJlvkPmCvb-a9BAA130_provenance.
- NP203056.RAa-dsL6p1dCNvGYGGIqUUMYSb3o7EJlvkPmCvb-a9BAA130_assertion wasDerivedFrom befree-20140225 NP203056.RAa-dsL6p1dCNvGYGGIqUUMYSb3o7EJlvkPmCvb-a9BAA130_provenance.
- NP203056.RAa-dsL6p1dCNvGYGGIqUUMYSb3o7EJlvkPmCvb-a9BAA130_assertion SIO_000772 7517218 NP203056.RAa-dsL6p1dCNvGYGGIqUUMYSb3o7EJlvkPmCvb-a9BAA130_provenance.
- NP203056.RAa-dsL6p1dCNvGYGGIqUUMYSb3o7EJlvkPmCvb-a9BAA130_assertion evidence source_evidence_literature NP203056.RAa-dsL6p1dCNvGYGGIqUUMYSb3o7EJlvkPmCvb-a9BAA130_provenance.
- NP203056.RAa-dsL6p1dCNvGYGGIqUUMYSb3o7EJlvkPmCvb-a9BAA130_assertion description "[Mutations of gp91phox cause X-linked CGD, whereas mutations of p22phox cause one of the three autosomal recessive forms of CGD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP203056.RAa-dsL6p1dCNvGYGGIqUUMYSb3o7EJlvkPmCvb-a9BAA130_provenance.