Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP804508.RAh9slNjpbYbXfZHGgGxDVSiYw2sM98LEwJnaMJgUmAXg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP804508.RAh9slNjpbYbXfZHGgGxDVSiYw2sM98LEwJnaMJgUmAXg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP804508.RAh9slNjpbYbXfZHGgGxDVSiYw2sM98LEwJnaMJgUmAXg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP804508.RAh9slNjpbYbXfZHGgGxDVSiYw2sM98LEwJnaMJgUmAXg130_provenance.
- NP804508.RAh9slNjpbYbXfZHGgGxDVSiYw2sM98LEwJnaMJgUmAXg130_assertion description "[Lesch-Nyhan disease (LND) is a rare X-linked recessive genetic disorder caused by a deficiency of hypoxanthine-guanine phosphoribosyltransferase (HPRT) enzyme.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP804508.RAh9slNjpbYbXfZHGgGxDVSiYw2sM98LEwJnaMJgUmAXg130_provenance.
- NP804508.RAh9slNjpbYbXfZHGgGxDVSiYw2sM98LEwJnaMJgUmAXg130_assertion evidence source_evidence_literature NP804508.RAh9slNjpbYbXfZHGgGxDVSiYw2sM98LEwJnaMJgUmAXg130_provenance.
- NP804508.RAh9slNjpbYbXfZHGgGxDVSiYw2sM98LEwJnaMJgUmAXg130_assertion SIO_000772 16826447 NP804508.RAh9slNjpbYbXfZHGgGxDVSiYw2sM98LEwJnaMJgUmAXg130_provenance.
- NP804508.RAh9slNjpbYbXfZHGgGxDVSiYw2sM98LEwJnaMJgUmAXg130_assertion wasDerivedFrom befree-20140225 NP804508.RAh9slNjpbYbXfZHGgGxDVSiYw2sM98LEwJnaMJgUmAXg130_provenance.
- NP804508.RAh9slNjpbYbXfZHGgGxDVSiYw2sM98LEwJnaMJgUmAXg130_assertion wasGeneratedBy ECO_0000203 NP804508.RAh9slNjpbYbXfZHGgGxDVSiYw2sM98LEwJnaMJgUmAXg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP804508.RAh9slNjpbYbXfZHGgGxDVSiYw2sM98LEwJnaMJgUmAXg130_provenance.