@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:NP1344986.RAOGcHL4j8grHAqB9pL7iMipkelVAVCb6h6hm-zVXGsh4130_head { this: np:hasAssertion dgn-np:NP1344986.RAOGcHL4j8grHAqB9pL7iMipkelVAVCb6h6hm-zVXGsh4130_assertion; np:hasProvenance dgn-np:NP1344986.RAOGcHL4j8grHAqB9pL7iMipkelVAVCb6h6hm-zVXGsh4130_provenance; np:hasPublicationInfo dgn-np:NP1344986.RAOGcHL4j8grHAqB9pL7iMipkelVAVCb6h6hm-zVXGsh4130_publicationInfo; a np:Nanopublication . dgn-np:NP1344986.RAOGcHL4j8grHAqB9pL7iMipkelVAVCb6h6hm-zVXGsh4130_assertion a np:Assertion . dgn-np:NP1344986.RAOGcHL4j8grHAqB9pL7iMipkelVAVCb6h6hm-zVXGsh4130_provenance a np:Provenance . dgn-np:NP1344986.RAOGcHL4j8grHAqB9pL7iMipkelVAVCb6h6hm-zVXGsh4130_publicationInfo a np:PublicationInfo . } dgn-np:NP1344986.RAOGcHL4j8grHAqB9pL7iMipkelVAVCb6h6hm-zVXGsh4130_assertion { miriam-gene:861 a ncit:C16612 . lld:C0023467 a ncit:C7057 . dgn-gda:DGNace4b7951dfdc5112acdcfd0bdf5d35c sio:SIO_000628 miriam-gene:861, lld:C0023467; a sio:SIO_001121 . } dgn-np:NP1344986.RAOGcHL4j8grHAqB9pL7iMipkelVAVCb6h6hm-zVXGsh4130_provenance { dgn-np:NP1344986.RAOGcHL4j8grHAqB9pL7iMipkelVAVCb6h6hm-zVXGsh4130_assertion dcterms:description "[In a study of 23 patients with t(8;21)-associated acute myeloid leukaemia the AML1-MTG8 fusion transcript was present in the majority of serial samples obtained from 17 patients followed for up to 34 months after diagnosis, but was absent in samples from all six patients who had been in continuous complete remission for 61 months after allogeneic bone marrow transplantation (BMT), or for 52, 53, 123, 182 and 198 months, respectively, after courses of intensive chemotherapy.]. 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:8547135; 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:NP1344986.RAOGcHL4j8grHAqB9pL7iMipkelVAVCb6h6hm-zVXGsh4130_publicationInfo { this: dcterms:created "2016-05-13T12:51:56+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" . }