Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP464527.RAYFojBNqrlRqviZ5WKsoojrTWpMb_pylDm8Ke45CXDi4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP464527.RAYFojBNqrlRqviZ5WKsoojrTWpMb_pylDm8Ke45CXDi4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP464527.RAYFojBNqrlRqviZ5WKsoojrTWpMb_pylDm8Ke45CXDi4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP464527.RAYFojBNqrlRqviZ5WKsoojrTWpMb_pylDm8Ke45CXDi4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP464527.RAYFojBNqrlRqviZ5WKsoojrTWpMb_pylDm8Ke45CXDi4130_provenance.
- 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.