@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:NP262987.RA9nnx-mYoPt7hmFSAsIpNaIiiY0bN7Sy2As5M952k0gc130_head { this: np:hasAssertion dgn-np:NP262987.RA9nnx-mYoPt7hmFSAsIpNaIiiY0bN7Sy2As5M952k0gc130_assertion; np:hasProvenance dgn-np:NP262987.RA9nnx-mYoPt7hmFSAsIpNaIiiY0bN7Sy2As5M952k0gc130_provenance; np:hasPublicationInfo dgn-np:NP262987.RA9nnx-mYoPt7hmFSAsIpNaIiiY0bN7Sy2As5M952k0gc130_publicationInfo; a np:Nanopublication . dgn-np:NP262987.RA9nnx-mYoPt7hmFSAsIpNaIiiY0bN7Sy2As5M952k0gc130_assertion a np:Assertion . dgn-np:NP262987.RA9nnx-mYoPt7hmFSAsIpNaIiiY0bN7Sy2As5M952k0gc130_provenance a np:Provenance . dgn-np:NP262987.RA9nnx-mYoPt7hmFSAsIpNaIiiY0bN7Sy2As5M952k0gc130_publicationInfo a np:PublicationInfo . } dgn-np:NP262987.RA9nnx-mYoPt7hmFSAsIpNaIiiY0bN7Sy2As5M952k0gc130_assertion { miriam-gene:596 a ncit:C16612 . lld:C0178874 a ncit:C7057 . dgn-gda:DGN9e53a863a6029f35b361e58dae780316 sio:SIO_000628 miriam-gene:596, lld:C0178874; a sio:SIO_001121 . } dgn-np:NP262987.RA9nnx-mYoPt7hmFSAsIpNaIiiY0bN7Sy2As5M952k0gc130_provenance { dgn-np:NP262987.RA9nnx-mYoPt7hmFSAsIpNaIiiY0bN7Sy2As5M952k0gc130_assertion dcterms:description "[Deregulation of apoptosis is one of the important features of AML and to understand the molecular mechanism underlying apoptosis and its contribution to tumor progression, this study aimed to evaluate anti-apoptotic Bcl2 protein expression in AML and correlate with FLT3 parameters for their role in prognosis of disease.Bcl2 and FLT3 protein expression was quantified by flow cytometry on leukemic blasts in total 174 de novo AML, myelodysplastic syndrome (MDS) and aplastic anemia patients.]. 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:23906301; prov:wasDerivedFrom dgn-void:befree-20150227; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP262987.RA9nnx-mYoPt7hmFSAsIpNaIiiY0bN7Sy2As5M952k0gc130_publicationInfo { this: dcterms:created "2015-08-25T14:40:09+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 "v3.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v3.0.0" . }