Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP596996.RAaNcJhFYExFlcTI2jYcwpMnvxacapBJvfiC7sG8WCrts130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP596996.RAaNcJhFYExFlcTI2jYcwpMnvxacapBJvfiC7sG8WCrts130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP596996.RAaNcJhFYExFlcTI2jYcwpMnvxacapBJvfiC7sG8WCrts130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP596996.RAaNcJhFYExFlcTI2jYcwpMnvxacapBJvfiC7sG8WCrts130_provenance.
- befree-20150227 importedOn "2015-02-27" NP596996.RAaNcJhFYExFlcTI2jYcwpMnvxacapBJvfiC7sG8WCrts130_provenance.
- 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.