Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP464474.RAiX-CtHMP10UEaz1s4EVnXRf3gD7gOocHbb8EX0Pwyik130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP464474.RAiX-CtHMP10UEaz1s4EVnXRf3gD7gOocHbb8EX0Pwyik130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP464474.RAiX-CtHMP10UEaz1s4EVnXRf3gD7gOocHbb8EX0Pwyik130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP464474.RAiX-CtHMP10UEaz1s4EVnXRf3gD7gOocHbb8EX0Pwyik130_provenance.
- NP464474.RAiX-CtHMP10UEaz1s4EVnXRf3gD7gOocHbb8EX0Pwyik130_assertion description "[Lesch-Nyhan disease (LND) is caused by congenital deficiency of the purine recycling enzyme, hypoxanthine-guanine phosphoribosyltransferase (HGprt).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP464474.RAiX-CtHMP10UEaz1s4EVnXRf3gD7gOocHbb8EX0Pwyik130_provenance.
- NP464474.RAiX-CtHMP10UEaz1s4EVnXRf3gD7gOocHbb8EX0Pwyik130_assertion evidence source_evidence_literature NP464474.RAiX-CtHMP10UEaz1s4EVnXRf3gD7gOocHbb8EX0Pwyik130_provenance.
- NP464474.RAiX-CtHMP10UEaz1s4EVnXRf3gD7gOocHbb8EX0Pwyik130_assertion SIO_000772 24891139 NP464474.RAiX-CtHMP10UEaz1s4EVnXRf3gD7gOocHbb8EX0Pwyik130_provenance.
- NP464474.RAiX-CtHMP10UEaz1s4EVnXRf3gD7gOocHbb8EX0Pwyik130_assertion wasDerivedFrom befree-20150227 NP464474.RAiX-CtHMP10UEaz1s4EVnXRf3gD7gOocHbb8EX0Pwyik130_provenance.
- NP464474.RAiX-CtHMP10UEaz1s4EVnXRf3gD7gOocHbb8EX0Pwyik130_assertion wasGeneratedBy ECO_0000203 NP464474.RAiX-CtHMP10UEaz1s4EVnXRf3gD7gOocHbb8EX0Pwyik130_provenance.
- befree-20150227 importedOn "2015-02-27" NP464474.RAiX-CtHMP10UEaz1s4EVnXRf3gD7gOocHbb8EX0Pwyik130_provenance.