Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP746567.RAllzrQuD71noUtCwhmuUOsm0icndstcwFHiboCvBrjjk130_assertion> ?p ?o ?g. }
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- NP746567.RAllzrQuD71noUtCwhmuUOsm0icndstcwFHiboCvBrjjk130_assertion type Assertion NP746567.RAllzrQuD71noUtCwhmuUOsm0icndstcwFHiboCvBrjjk130_head.
- NP746567.RAllzrQuD71noUtCwhmuUOsm0icndstcwFHiboCvBrjjk130_assertion wasGeneratedBy ECO_0000203 NP746567.RAllzrQuD71noUtCwhmuUOsm0icndstcwFHiboCvBrjjk130_provenance.
- NP746567.RAllzrQuD71noUtCwhmuUOsm0icndstcwFHiboCvBrjjk130_assertion wasDerivedFrom befree-20140225 NP746567.RAllzrQuD71noUtCwhmuUOsm0icndstcwFHiboCvBrjjk130_provenance.
- NP746567.RAllzrQuD71noUtCwhmuUOsm0icndstcwFHiboCvBrjjk130_assertion SIO_000772 23371835 NP746567.RAllzrQuD71noUtCwhmuUOsm0icndstcwFHiboCvBrjjk130_provenance.
- NP746567.RAllzrQuD71noUtCwhmuUOsm0icndstcwFHiboCvBrjjk130_assertion evidence source_evidence_literature NP746567.RAllzrQuD71noUtCwhmuUOsm0icndstcwFHiboCvBrjjk130_provenance.
- 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.