@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:NP1103096.RAkF7DOYoWw11zp2n6lA2wMMHeWJ41n4lASG3p_iQ7G0E130_head { this: np:hasAssertion dgn-np:NP1103096.RAkF7DOYoWw11zp2n6lA2wMMHeWJ41n4lASG3p_iQ7G0E130_assertion; np:hasProvenance dgn-np:NP1103096.RAkF7DOYoWw11zp2n6lA2wMMHeWJ41n4lASG3p_iQ7G0E130_provenance; np:hasPublicationInfo dgn-np:NP1103096.RAkF7DOYoWw11zp2n6lA2wMMHeWJ41n4lASG3p_iQ7G0E130_publicationInfo; a np:Nanopublication . dgn-np:NP1103096.RAkF7DOYoWw11zp2n6lA2wMMHeWJ41n4lASG3p_iQ7G0E130_assertion a np:Assertion . dgn-np:NP1103096.RAkF7DOYoWw11zp2n6lA2wMMHeWJ41n4lASG3p_iQ7G0E130_provenance a np:Provenance . dgn-np:NP1103096.RAkF7DOYoWw11zp2n6lA2wMMHeWJ41n4lASG3p_iQ7G0E130_publicationInfo a np:PublicationInfo . } dgn-np:NP1103096.RAkF7DOYoWw11zp2n6lA2wMMHeWJ41n4lASG3p_iQ7G0E130_assertion { miriam-gene:2896 a ncit:C16612 . lld:C0026764 a ncit:C7057 . dgn-gda:DGNa26f6d1f946fc25b24ebf0848d4df8c1 sio:SIO_000628 miriam-gene:2896, lld:C0026764; a sio:SIO_001121 . } dgn-np:NP1103096.RAkF7DOYoWw11zp2n6lA2wMMHeWJ41n4lASG3p_iQ7G0E130_provenance { dgn-np:NP1103096.RAkF7DOYoWw11zp2n6lA2wMMHeWJ41n4lASG3p_iQ7G0E130_assertion dcterms:description "[Classic prognostic parameters and qPCR-based GEP predicted MM patient outcome and, although multivariate analyses revealed that cytogenetic risk (standard vs. high risk) was the variable that most strongly predicted prognosis, GEP added significant information for risk stratification.]. 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:23952215; 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:NP1103096.RAkF7DOYoWw11zp2n6lA2wMMHeWJ41n4lASG3p_iQ7G0E130_publicationInfo { this: dcterms:created "2016-05-13T12:50:06+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" . }