Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP596996.RAaNcJhFYExFlcTI2jYcwpMnvxacapBJvfiC7sG8WCrts130_assertion> ?p ?o ?g. }
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- NP596996.RAaNcJhFYExFlcTI2jYcwpMnvxacapBJvfiC7sG8WCrts130_assertion type Assertion NP596996.RAaNcJhFYExFlcTI2jYcwpMnvxacapBJvfiC7sG8WCrts130_head.
- NP596996.RAaNcJhFYExFlcTI2jYcwpMnvxacapBJvfiC7sG8WCrts130_assertion wasGeneratedBy ECO_0000203 NP596996.RAaNcJhFYExFlcTI2jYcwpMnvxacapBJvfiC7sG8WCrts130_provenance.
- NP596996.RAaNcJhFYExFlcTI2jYcwpMnvxacapBJvfiC7sG8WCrts130_assertion wasDerivedFrom befree-20150227 NP596996.RAaNcJhFYExFlcTI2jYcwpMnvxacapBJvfiC7sG8WCrts130_provenance.
- NP596996.RAaNcJhFYExFlcTI2jYcwpMnvxacapBJvfiC7sG8WCrts130_assertion SIO_000772 23371835 NP596996.RAaNcJhFYExFlcTI2jYcwpMnvxacapBJvfiC7sG8WCrts130_provenance.
- NP596996.RAaNcJhFYExFlcTI2jYcwpMnvxacapBJvfiC7sG8WCrts130_assertion evidence source_evidence_literature NP596996.RAaNcJhFYExFlcTI2jYcwpMnvxacapBJvfiC7sG8WCrts130_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.