@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:NP374287.RAnXGcFZsM6CnEpEu6-ZBekS-nj7xUHGErA7gxP9fVmJ0130_head { this: np:hasAssertion dgn-np:NP374287.RAnXGcFZsM6CnEpEu6-ZBekS-nj7xUHGErA7gxP9fVmJ0130_assertion; np:hasProvenance dgn-np:NP374287.RAnXGcFZsM6CnEpEu6-ZBekS-nj7xUHGErA7gxP9fVmJ0130_provenance; np:hasPublicationInfo dgn-np:NP374287.RAnXGcFZsM6CnEpEu6-ZBekS-nj7xUHGErA7gxP9fVmJ0130_publicationInfo; a np:Nanopublication . dgn-np:NP374287.RAnXGcFZsM6CnEpEu6-ZBekS-nj7xUHGErA7gxP9fVmJ0130_assertion a np:Assertion . dgn-np:NP374287.RAnXGcFZsM6CnEpEu6-ZBekS-nj7xUHGErA7gxP9fVmJ0130_provenance a np:Provenance . dgn-np:NP374287.RAnXGcFZsM6CnEpEu6-ZBekS-nj7xUHGErA7gxP9fVmJ0130_publicationInfo a np:PublicationInfo . } dgn-np:NP374287.RAnXGcFZsM6CnEpEu6-ZBekS-nj7xUHGErA7gxP9fVmJ0130_assertion { miriam-gene:377677 a ncit:C16612 . lld:C0008626 a ncit:C7057 . dgn-gda:DGN0cd61db448e57a7136a2d1998d137569 sio:SIO_000628 miriam-gene:377677, lld:C0008626; a sio:SIO_001121 . } dgn-np:NP374287.RAnXGcFZsM6CnEpEu6-ZBekS-nj7xUHGErA7gxP9fVmJ0130_provenance { dgn-np:NP374287.RAnXGcFZsM6CnEpEu6-ZBekS-nj7xUHGErA7gxP9fVmJ0130_assertion dcterms:description "[Long-term follow-up on Total Therapy I revealed, with a median follow-up of about 10 years, median durations of event-free survival (EFS) and overall survival (OS) of 37 and 80 mos in the 88% of patients lacking cytogenetic abnormalities (CA) of chromosome 13 compared to only 28 and 34 mos in those with CA 13.]. 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:12430877; 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:NP374287.RAnXGcFZsM6CnEpEu6-ZBekS-nj7xUHGErA7gxP9fVmJ0130_publicationInfo { this: dcterms:created "2016-05-13T12:44:35+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" . }