@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:NP1186215.RAcjbS4kccczWcOjr_XmsUihyIAlSwjJMKeXnO-ki06rs130_head { this: np:hasAssertion dgn-np:NP1186215.RAcjbS4kccczWcOjr_XmsUihyIAlSwjJMKeXnO-ki06rs130_assertion; np:hasProvenance dgn-np:NP1186215.RAcjbS4kccczWcOjr_XmsUihyIAlSwjJMKeXnO-ki06rs130_provenance; np:hasPublicationInfo dgn-np:NP1186215.RAcjbS4kccczWcOjr_XmsUihyIAlSwjJMKeXnO-ki06rs130_publicationInfo; a np:Nanopublication . dgn-np:NP1186215.RAcjbS4kccczWcOjr_XmsUihyIAlSwjJMKeXnO-ki06rs130_assertion a np:Assertion . dgn-np:NP1186215.RAcjbS4kccczWcOjr_XmsUihyIAlSwjJMKeXnO-ki06rs130_provenance a np:Provenance . dgn-np:NP1186215.RAcjbS4kccczWcOjr_XmsUihyIAlSwjJMKeXnO-ki06rs130_publicationInfo a np:PublicationInfo . } dgn-np:NP1186215.RAcjbS4kccczWcOjr_XmsUihyIAlSwjJMKeXnO-ki06rs130_assertion { miriam-gene:3418 a ncit:C16612 . lld:C0023467 a ncit:C7057 . dgn-gda:DGNeed5e3f6f991b2cbbef0f5e7b2278722 sio:SIO_000628 miriam-gene:3418, lld:C0023467; a sio:SIO_001121 . } dgn-np:NP1186215.RAcjbS4kccczWcOjr_XmsUihyIAlSwjJMKeXnO-ki06rs130_provenance { dgn-np:NP1186215.RAcjbS4kccczWcOjr_XmsUihyIAlSwjJMKeXnO-ki06rs130_assertion dcterms:description "[Firstly, by analyzing biomarkers associated with AML, to assist normal clinical tests, we confirmed that the patient was anormal karyo type, with NPM1 and IDH2 mutations and deregulation patterns of related genes, such as BAALC, ERG, MN1 and HOX family.]. 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:24867525; 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:NP1186215.RAcjbS4kccczWcOjr_XmsUihyIAlSwjJMKeXnO-ki06rs130_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" . }