@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:NP1305798.RAkpvsSRjTbF_KgihMNyjyLmGsghPey3j3r3kmi1aJEgM130_head { this: np:hasAssertion dgn-np:NP1305798.RAkpvsSRjTbF_KgihMNyjyLmGsghPey3j3r3kmi1aJEgM130_assertion; np:hasProvenance dgn-np:NP1305798.RAkpvsSRjTbF_KgihMNyjyLmGsghPey3j3r3kmi1aJEgM130_provenance; np:hasPublicationInfo dgn-np:NP1305798.RAkpvsSRjTbF_KgihMNyjyLmGsghPey3j3r3kmi1aJEgM130_publicationInfo; a np:Nanopublication . dgn-np:NP1305798.RAkpvsSRjTbF_KgihMNyjyLmGsghPey3j3r3kmi1aJEgM130_assertion a np:Assertion . dgn-np:NP1305798.RAkpvsSRjTbF_KgihMNyjyLmGsghPey3j3r3kmi1aJEgM130_provenance a np:Provenance . dgn-np:NP1305798.RAkpvsSRjTbF_KgihMNyjyLmGsghPey3j3r3kmi1aJEgM130_publicationInfo a np:PublicationInfo . } dgn-np:NP1305798.RAkpvsSRjTbF_KgihMNyjyLmGsghPey3j3r3kmi1aJEgM130_assertion { miriam-gene:2187 a ncit:C16612 . lld:C0023418 a ncit:C7057 . dgn-gda:DGNabe4aa6c78f654354a4a956fafc40826 sio:SIO_000628 miriam-gene:2187, lld:C0023418; a sio:SIO_001121 . } dgn-np:NP1305798.RAkpvsSRjTbF_KgihMNyjyLmGsghPey3j3r3kmi1aJEgM130_provenance { dgn-np:NP1305798.RAkpvsSRjTbF_KgihMNyjyLmGsghPey3j3r3kmi1aJEgM130_assertion dcterms:description "[Although leukemia with this chromosomal abnormality has been classified as L2 acute lymphoblastic leukemia by the FAB classification, two of our cases appeared to be of myelomonocyte origin as demonstrated by cytochemical, immunologic, and electron microscopic studies and differentiation induction by 12-tetradecanoyl-phorbol-13-acetate and methylformamide.]. 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:6340755; 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:NP1305798.RAkpvsSRjTbF_KgihMNyjyLmGsghPey3j3r3kmi1aJEgM130_publicationInfo { this: dcterms:created "2016-05-13T12:51:38+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" . }