Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP318662.RAyk66Y6lbGQ0Rg-3QEAAfDJjAGBkLYRYCNj59S8z6XhQ130_assertion> ?p ?o ?g. }
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- NP318662.RAyk66Y6lbGQ0Rg-3QEAAfDJjAGBkLYRYCNj59S8z6XhQ130_assertion type Assertion NP318662.RAyk66Y6lbGQ0Rg-3QEAAfDJjAGBkLYRYCNj59S8z6XhQ130_head.
- NP318662.RAyk66Y6lbGQ0Rg-3QEAAfDJjAGBkLYRYCNj59S8z6XhQ130_assertion wasGeneratedBy ECO_0000203 NP318662.RAyk66Y6lbGQ0Rg-3QEAAfDJjAGBkLYRYCNj59S8z6XhQ130_provenance.
- NP318662.RAyk66Y6lbGQ0Rg-3QEAAfDJjAGBkLYRYCNj59S8z6XhQ130_assertion wasDerivedFrom befree-2016 NP318662.RAyk66Y6lbGQ0Rg-3QEAAfDJjAGBkLYRYCNj59S8z6XhQ130_provenance.
- NP318662.RAyk66Y6lbGQ0Rg-3QEAAfDJjAGBkLYRYCNj59S8z6XhQ130_assertion SIO_000772 11369620 NP318662.RAyk66Y6lbGQ0Rg-3QEAAfDJjAGBkLYRYCNj59S8z6XhQ130_provenance.
- NP318662.RAyk66Y6lbGQ0Rg-3QEAAfDJjAGBkLYRYCNj59S8z6XhQ130_assertion evidence source_evidence_literature NP318662.RAyk66Y6lbGQ0Rg-3QEAAfDJjAGBkLYRYCNj59S8z6XhQ130_provenance.
- NP318662.RAyk66Y6lbGQ0Rg-3QEAAfDJjAGBkLYRYCNj59S8z6XhQ130_assertion description "[Pyrimidine 5' nucleotidase (P5'N-1) deficiency is an autosomal recessive condition causing hemolytic anemia characterized by marked basophilic stippling and the accumulation of high concentrations of pyrimidine nucleotides within the erythrocyte.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP318662.RAyk66Y6lbGQ0Rg-3QEAAfDJjAGBkLYRYCNj59S8z6XhQ130_provenance.