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<http://rdf.disgenet.org/gene-disease-association.ttl#DGN1cf0f3ca5fc2ce0c073371073b46fb6d> <http://semanticscience.org/resource/SIO_000628> <http://linkedlifedata.com/resource/umls/id/C0022661> <http://rdf.disgenet.org/nanopublications.trig#NP216677.RAQNVaFmVKZzPVlM3JFPTsTJjR6u7Dn8llt4W_uR_jeCw130_assertion> .
<http://rdf.disgenet.org/gene-disease-association.ttl#DGN1cf0f3ca5fc2ce0c073371073b46fb6d> <http://www.w3.org/1999/02/22-rdf-syntax-ns#type> <http://semanticscience.org/resource/SIO_001121> <http://rdf.disgenet.org/nanopublications.trig#NP216677.RAQNVaFmVKZzPVlM3JFPTsTJjR6u7Dn8llt4W_uR_jeCw130_assertion> .
<http://rdf.disgenet.org/nanopublications.trig#NP216677.RAQNVaFmVKZzPVlM3JFPTsTJjR6u7Dn8llt4W_uR_jeCw130_assertion> <http://purl.org/dc/terms/description> "[In humans, adenine phosphoribosyltransferase (APRT, EC 2.4.2.7) deficiency can manifest as nephrolithiasis, interstitial nephritis, and chronic renal failure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en <http://rdf.disgenet.org/nanopublications.trig#NP216677.RAQNVaFmVKZzPVlM3JFPTsTJjR6u7Dn8llt4W_uR_jeCw130_provenance> .
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<http://rdf.disgenet.org/v2.1.0/void.ttl#befree-20140225> <http://purl.org/pav/2.0/importedOn> "2014-02-25"^^<http://www.w3.org/2001/XMLSchema#date> <http://rdf.disgenet.org/nanopublications.trig#NP216677.RAQNVaFmVKZzPVlM3JFPTsTJjR6u7Dn8llt4W_uR_jeCw130_provenance> .
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<http://rdf.disgenet.org/v2.1.0/void.ttl#source_evidence_literature> <http://www.w3.org/2000/01/rdf-schema#comment> "Gene-disease associations inferred from text-mining the literature."@en <http://rdf.disgenet.org/nanopublications.trig#NP216677.RAQNVaFmVKZzPVlM3JFPTsTJjR6u7Dn8llt4W_uR_jeCw130_provenance> .
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