Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1244925.RAVXe5kWJVJLgmTzXYtBoxMVi8Ymid6HUrw8rO8V8vPzk130_assertion> ?p ?o ?g. }
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- NP1244925.RAVXe5kWJVJLgmTzXYtBoxMVi8Ymid6HUrw8rO8V8vPzk130_assertion type Assertion NP1244925.RAVXe5kWJVJLgmTzXYtBoxMVi8Ymid6HUrw8rO8V8vPzk130_head.
- NP1244925.RAVXe5kWJVJLgmTzXYtBoxMVi8Ymid6HUrw8rO8V8vPzk130_assertion description "[X-linked hypoxanthine-guanine phosphoribosyltransferase (HPRT) deficiency in an inherited disorder of purine metabolism is usually associated with the clinical manifestations of hyperuricemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1244925.RAVXe5kWJVJLgmTzXYtBoxMVi8Ymid6HUrw8rO8V8vPzk130_provenance.
- NP1244925.RAVXe5kWJVJLgmTzXYtBoxMVi8Ymid6HUrw8rO8V8vPzk130_assertion evidence source_evidence_literature NP1244925.RAVXe5kWJVJLgmTzXYtBoxMVi8Ymid6HUrw8rO8V8vPzk130_provenance.
- NP1244925.RAVXe5kWJVJLgmTzXYtBoxMVi8Ymid6HUrw8rO8V8vPzk130_assertion SIO_000772 25476133 NP1244925.RAVXe5kWJVJLgmTzXYtBoxMVi8Ymid6HUrw8rO8V8vPzk130_provenance.
- NP1244925.RAVXe5kWJVJLgmTzXYtBoxMVi8Ymid6HUrw8rO8V8vPzk130_assertion wasDerivedFrom befree-2016 NP1244925.RAVXe5kWJVJLgmTzXYtBoxMVi8Ymid6HUrw8rO8V8vPzk130_provenance.
- NP1244925.RAVXe5kWJVJLgmTzXYtBoxMVi8Ymid6HUrw8rO8V8vPzk130_assertion wasGeneratedBy ECO_0000203 NP1244925.RAVXe5kWJVJLgmTzXYtBoxMVi8Ymid6HUrw8rO8V8vPzk130_provenance.