Matches in Nanopublications for { ?s ?p "[Purine nucleoside phosphorylase (PNP) deficiency is an autosomal recessive genetic disorder of the purine salvage pathway, associated with a variable extent of immunodeficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP746567.RAllzrQuD71noUtCwhmuUOsm0icndstcwFHiboCvBrjjk130_assertion description "[Purine nucleoside phosphorylase (PNP) deficiency is an autosomal recessive genetic disorder of the purine salvage pathway, associated with a variable extent of immunodeficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP746567.RAllzrQuD71noUtCwhmuUOsm0icndstcwFHiboCvBrjjk130_provenance.
- NP596996.RAaNcJhFYExFlcTI2jYcwpMnvxacapBJvfiC7sG8WCrts130_assertion description "[Purine nucleoside phosphorylase (PNP) deficiency is an autosomal recessive genetic disorder of the purine salvage pathway, associated with a variable extent of immunodeficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP596996.RAaNcJhFYExFlcTI2jYcwpMnvxacapBJvfiC7sG8WCrts130_provenance.