@prefix this: . @prefix rdfs: . @prefix xsd: . @prefix sio: . @prefix ncit: . @prefix lld: . @prefix miriam-gene: . @prefix miriam-pubmed: . @prefix eco: . @prefix wi: . @prefix prov: . @prefix pav: . @prefix prv: . @prefix dcterms: . @prefix np: . @prefix dgn-np: . @prefix dgn-gda: . @prefix dgn-void: . dgn-np:NP295091.RAPPqvHdyXfuOkA9t2YvDHpJsh165_fmV9nYLRx4UrFlY130_head { this: np:hasAssertion dgn-np:NP295091.RAPPqvHdyXfuOkA9t2YvDHpJsh165_fmV9nYLRx4UrFlY130_assertion; np:hasProvenance dgn-np:NP295091.RAPPqvHdyXfuOkA9t2YvDHpJsh165_fmV9nYLRx4UrFlY130_provenance; np:hasPublicationInfo dgn-np:NP295091.RAPPqvHdyXfuOkA9t2YvDHpJsh165_fmV9nYLRx4UrFlY130_publicationInfo; a np:Nanopublication . dgn-np:NP295091.RAPPqvHdyXfuOkA9t2YvDHpJsh165_fmV9nYLRx4UrFlY130_assertion a np:Assertion . dgn-np:NP295091.RAPPqvHdyXfuOkA9t2YvDHpJsh165_fmV9nYLRx4UrFlY130_provenance a np:Provenance . dgn-np:NP295091.RAPPqvHdyXfuOkA9t2YvDHpJsh165_fmV9nYLRx4UrFlY130_publicationInfo a np:PublicationInfo . } dgn-np:NP295091.RAPPqvHdyXfuOkA9t2YvDHpJsh165_fmV9nYLRx4UrFlY130_assertion { miriam-gene:3251 a ncit:C16612 . lld:C0596263 a ncit:C7057 . dgn-gda:DGN806a3e815631f46e59b5a2447d7f014e sio:SIO_000628 miriam-gene:3251, lld:C0596263; a sio:SIO_001121 . } dgn-np:NP295091.RAPPqvHdyXfuOkA9t2YvDHpJsh165_fmV9nYLRx4UrFlY130_provenance { dgn-np:NP295091.RAPPqvHdyXfuOkA9t2YvDHpJsh165_fmV9nYLRx4UrFlY130_assertion dcterms:description "[The specificity of mutations induced by PhIP exposure at the endogenous HPRT locus was determined in cell lines defective in MMR to better understand the mutagenic effects of PhIP in MMR-defective individuals and to gain insight into the molecular mechanism of carcinogenesis induced by PhIP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en; wi:evidence dgn-void:source_evidence_literature; sio:SIO_000772 miriam-pubmed:10987307; prov:wasDerivedFrom dgn-void:befree-2016; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-2016 pav:importedOn "2016-02-19"^^xsd:date . dgn-void:source_evidence_literature a eco:ECO_0000212; rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en; rdfs:label "DisGeNET evidence - LITERATURE"@en . } dgn-np:NP295091.RAPPqvHdyXfuOkA9t2YvDHpJsh165_fmV9nYLRx4UrFlY130_publicationInfo { this: dcterms:created "2016-05-13T12:43:59+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetv3.0rdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v4.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v4.0.0" . }