@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:NP1186599.RAtoLM7_7MFuAXclptIwGtn0fF9QZIgzYmGfeb2-M17Ns130_head { this: np:hasAssertion dgn-np:NP1186599.RAtoLM7_7MFuAXclptIwGtn0fF9QZIgzYmGfeb2-M17Ns130_assertion; np:hasProvenance dgn-np:NP1186599.RAtoLM7_7MFuAXclptIwGtn0fF9QZIgzYmGfeb2-M17Ns130_provenance; np:hasPublicationInfo dgn-np:NP1186599.RAtoLM7_7MFuAXclptIwGtn0fF9QZIgzYmGfeb2-M17Ns130_publicationInfo; a np:Nanopublication . dgn-np:NP1186599.RAtoLM7_7MFuAXclptIwGtn0fF9QZIgzYmGfeb2-M17Ns130_assertion a np:Assertion . dgn-np:NP1186599.RAtoLM7_7MFuAXclptIwGtn0fF9QZIgzYmGfeb2-M17Ns130_provenance a np:Provenance . dgn-np:NP1186599.RAtoLM7_7MFuAXclptIwGtn0fF9QZIgzYmGfeb2-M17Ns130_publicationInfo a np:PublicationInfo . } dgn-np:NP1186599.RAtoLM7_7MFuAXclptIwGtn0fF9QZIgzYmGfeb2-M17Ns130_assertion { miriam-gene:7422 a ncit:C16612 . lld:C0017638 a ncit:C7057 . dgn-gda:DGNa001504155897e4c9d4343aa256401f4 sio:SIO_000628 miriam-gene:7422, lld:C0017638; a sio:SIO_001121 . } dgn-np:NP1186599.RAtoLM7_7MFuAXclptIwGtn0fF9QZIgzYmGfeb2-M17Ns130_provenance { dgn-np:NP1186599.RAtoLM7_7MFuAXclptIwGtn0fF9QZIgzYmGfeb2-M17Ns130_assertion dcterms:description "[Using the World Health Organization grade, histological subtype, and molecular variants (1p/19q codeletion, isocitrate dehydrogenase 1/2 mutation, Ki-67 index, O6-methylguanine DNA methyltransferase, P53, and vascular endothelial growth factor immunoactivity) as prognostic biomarkers, we performed receiver operating characteristic analysis and multiple linear regression to assess the association between the magnetic resonance diffusion parameter and mean ADC and the prognostic factors of glioma pathology.]. 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:24874469; 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:NP1186599.RAtoLM7_7MFuAXclptIwGtn0fF9QZIgzYmGfeb2-M17Ns130_publicationInfo { this: dcterms:created "2016-05-13T12:50:43+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" . }