@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:NP466942.RAytN_1JreONW_jtV9u5B5uJa7T7HC6O1E3pddGDmsIe8130_head { this: np:hasAssertion dgn-np:NP466942.RAytN_1JreONW_jtV9u5B5uJa7T7HC6O1E3pddGDmsIe8130_assertion; np:hasProvenance dgn-np:NP466942.RAytN_1JreONW_jtV9u5B5uJa7T7HC6O1E3pddGDmsIe8130_provenance; np:hasPublicationInfo dgn-np:NP466942.RAytN_1JreONW_jtV9u5B5uJa7T7HC6O1E3pddGDmsIe8130_publicationInfo; a np:Nanopublication . dgn-np:NP466942.RAytN_1JreONW_jtV9u5B5uJa7T7HC6O1E3pddGDmsIe8130_assertion a np:Assertion . dgn-np:NP466942.RAytN_1JreONW_jtV9u5B5uJa7T7HC6O1E3pddGDmsIe8130_provenance a np:Provenance . dgn-np:NP466942.RAytN_1JreONW_jtV9u5B5uJa7T7HC6O1E3pddGDmsIe8130_publicationInfo a np:PublicationInfo . } dgn-np:NP466942.RAytN_1JreONW_jtV9u5B5uJa7T7HC6O1E3pddGDmsIe8130_assertion { miriam-gene:3304 a ncit:C16612 . lld:C0262655 a ncit:C7057 . dgn-gda:DGNa4f0d25a10ea2d287d3b9bacca86133e sio:SIO_000628 miriam-gene:3304, lld:C0262655; a sio:SIO_001121 . } dgn-np:NP466942.RAytN_1JreONW_jtV9u5B5uJa7T7HC6O1E3pddGDmsIe8130_provenance { dgn-np:NP466942.RAytN_1JreONW_jtV9u5B5uJa7T7HC6O1E3pddGDmsIe8130_assertion dcterms:description "[Our data indicates a relationship between the carrier status of HSPA1B (1267)G and TLR4 (896)G alleles and the development of recurrent UTI in childhood independently of other renal abnormalities, while raising further questions about the clinical and therapeutic relevance of these polymorphisms in everyday pediatric nephrology.]. 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:17314700; prov:wasDerivedFrom dgn-void:befree-20150227; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP466942.RAytN_1JreONW_jtV9u5B5uJa7T7HC6O1E3pddGDmsIe8130_publicationInfo { this: dcterms:created "2015-08-25T14:42:14+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 "v3.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v3.0.0" . }