Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP464527.RAYFojBNqrlRqviZ5WKsoojrTWpMb_pylDm8Ke45CXDi4130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP464527.RAYFojBNqrlRqviZ5WKsoojrTWpMb_pylDm8Ke45CXDi4130_assertion type Assertion NP464527.RAYFojBNqrlRqviZ5WKsoojrTWpMb_pylDm8Ke45CXDi4130_head.
- NP464527.RAYFojBNqrlRqviZ5WKsoojrTWpMb_pylDm8Ke45CXDi4130_assertion wasGeneratedBy ECO_0000203 NP464527.RAYFojBNqrlRqviZ5WKsoojrTWpMb_pylDm8Ke45CXDi4130_provenance.
- NP464527.RAYFojBNqrlRqviZ5WKsoojrTWpMb_pylDm8Ke45CXDi4130_assertion wasDerivedFrom befree-20150227 NP464527.RAYFojBNqrlRqviZ5WKsoojrTWpMb_pylDm8Ke45CXDi4130_provenance.
- NP464527.RAYFojBNqrlRqviZ5WKsoojrTWpMb_pylDm8Ke45CXDi4130_assertion SIO_000772 23804752 NP464527.RAYFojBNqrlRqviZ5WKsoojrTWpMb_pylDm8Ke45CXDi4130_provenance.
- NP464527.RAYFojBNqrlRqviZ5WKsoojrTWpMb_pylDm8Ke45CXDi4130_assertion evidence source_evidence_literature NP464527.RAYFojBNqrlRqviZ5WKsoojrTWpMb_pylDm8Ke45CXDi4130_provenance.
- NP464527.RAYFojBNqrlRqviZ5WKsoojrTWpMb_pylDm8Ke45CXDi4130_assertion description "[Lesch-Nyhan syndrome (LNS) is a neurodevelopmental disorder caused by mutations in the gene encoding the purine metabolic enzyme hypoxanthine-guanine phosphoribosyltransferase (HPRT).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP464527.RAYFojBNqrlRqviZ5WKsoojrTWpMb_pylDm8Ke45CXDi4130_provenance.