@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:NP1160648.RAKhqSljdt1zhKuru-xWVTIvB_5NNiCemQjR97HLZ-QqQ130_head { this: np:hasAssertion dgn-np:NP1160648.RAKhqSljdt1zhKuru-xWVTIvB_5NNiCemQjR97HLZ-QqQ130_assertion; np:hasProvenance dgn-np:NP1160648.RAKhqSljdt1zhKuru-xWVTIvB_5NNiCemQjR97HLZ-QqQ130_provenance; np:hasPublicationInfo dgn-np:NP1160648.RAKhqSljdt1zhKuru-xWVTIvB_5NNiCemQjR97HLZ-QqQ130_publicationInfo; a np:Nanopublication . dgn-np:NP1160648.RAKhqSljdt1zhKuru-xWVTIvB_5NNiCemQjR97HLZ-QqQ130_assertion a np:Assertion . dgn-np:NP1160648.RAKhqSljdt1zhKuru-xWVTIvB_5NNiCemQjR97HLZ-QqQ130_provenance a np:Provenance . dgn-np:NP1160648.RAKhqSljdt1zhKuru-xWVTIvB_5NNiCemQjR97HLZ-QqQ130_publicationInfo a np:PublicationInfo . } dgn-np:NP1160648.RAKhqSljdt1zhKuru-xWVTIvB_5NNiCemQjR97HLZ-QqQ130_assertion { miriam-gene:10320 a ncit:C16612 . lld:C1961102 a ncit:C7057 . dgn-gda:DGNe2d6dde4096e27d25b74b304c79bccc3 sio:SIO_000628 miriam-gene:10320, lld:C1961102; a sio:SIO_001122 . } dgn-np:NP1160648.RAKhqSljdt1zhKuru-xWVTIvB_5NNiCemQjR97HLZ-QqQ130_provenance { dgn-np:NP1160648.RAKhqSljdt1zhKuru-xWVTIvB_5NNiCemQjR97HLZ-QqQ130_assertion dcterms:description "[Since recently conducted genome-wide association (GWA) studies revealed that the common low-penetrance susceptibility allele at 7p12.2 (IKZF1 gene) confers an increased risk of pediatric ALL, we investigated whether the risk allele at rs4132601 also coexists with well-established prognostic factors, among 508 Polish pediatric patients with newly diagnosed ALL.]. 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:24597983; 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:NP1160648.RAKhqSljdt1zhKuru-xWVTIvB_5NNiCemQjR97HLZ-QqQ130_publicationInfo { this: dcterms:created "2016-05-13T12:50:32+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" . }