Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP804965.RA5Nk3SMfiOuox5LR_Zl9lBDsdS9kPmDhkc4ow3vcgz8k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP804965.RA5Nk3SMfiOuox5LR_Zl9lBDsdS9kPmDhkc4ow3vcgz8k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP804965.RA5Nk3SMfiOuox5LR_Zl9lBDsdS9kPmDhkc4ow3vcgz8k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP804965.RA5Nk3SMfiOuox5LR_Zl9lBDsdS9kPmDhkc4ow3vcgz8k130_provenance.
- NP804965.RA5Nk3SMfiOuox5LR_Zl9lBDsdS9kPmDhkc4ow3vcgz8k130_assertion wasGeneratedBy ECO_0000203 NP804965.RA5Nk3SMfiOuox5LR_Zl9lBDsdS9kPmDhkc4ow3vcgz8k130_provenance.
- NP804965.RA5Nk3SMfiOuox5LR_Zl9lBDsdS9kPmDhkc4ow3vcgz8k130_assertion wasDerivedFrom befree-20140225 NP804965.RA5Nk3SMfiOuox5LR_Zl9lBDsdS9kPmDhkc4ow3vcgz8k130_provenance.
- NP804965.RA5Nk3SMfiOuox5LR_Zl9lBDsdS9kPmDhkc4ow3vcgz8k130_assertion SIO_000772 22212387 NP804965.RA5Nk3SMfiOuox5LR_Zl9lBDsdS9kPmDhkc4ow3vcgz8k130_provenance.
- NP804965.RA5Nk3SMfiOuox5LR_Zl9lBDsdS9kPmDhkc4ow3vcgz8k130_assertion evidence source_evidence_literature NP804965.RA5Nk3SMfiOuox5LR_Zl9lBDsdS9kPmDhkc4ow3vcgz8k130_provenance.
- NP804965.RA5Nk3SMfiOuox5LR_Zl9lBDsdS9kPmDhkc4ow3vcgz8k130_assertion description "[Adenine phosphoribosyltransferase (APRT) deficiency is a rare autosomal recessive disorder characterized by 2,8-dihydroxyadenine (2,8-DHA) crystalluria that can cause nephrolithiasis and chronic kidney disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP804965.RA5Nk3SMfiOuox5LR_Zl9lBDsdS9kPmDhkc4ow3vcgz8k130_provenance.
- befree-20140225 importedOn "2014-02-25" NP804965.RA5Nk3SMfiOuox5LR_Zl9lBDsdS9kPmDhkc4ow3vcgz8k130_provenance.