@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:NP1409217.RAg4u3HW-pCF-OWL46PKVcl7mB0GKtzJe-VcxSHuFr_Ag130_head { this: np:hasAssertion dgn-np:NP1409217.RAg4u3HW-pCF-OWL46PKVcl7mB0GKtzJe-VcxSHuFr_Ag130_assertion; np:hasProvenance dgn-np:NP1409217.RAg4u3HW-pCF-OWL46PKVcl7mB0GKtzJe-VcxSHuFr_Ag130_provenance; np:hasPublicationInfo dgn-np:NP1409217.RAg4u3HW-pCF-OWL46PKVcl7mB0GKtzJe-VcxSHuFr_Ag130_publicationInfo; a np:Nanopublication . dgn-np:NP1409217.RAg4u3HW-pCF-OWL46PKVcl7mB0GKtzJe-VcxSHuFr_Ag130_assertion a np:Assertion . dgn-np:NP1409217.RAg4u3HW-pCF-OWL46PKVcl7mB0GKtzJe-VcxSHuFr_Ag130_provenance a np:Provenance . dgn-np:NP1409217.RAg4u3HW-pCF-OWL46PKVcl7mB0GKtzJe-VcxSHuFr_Ag130_publicationInfo a np:PublicationInfo . } dgn-np:NP1409217.RAg4u3HW-pCF-OWL46PKVcl7mB0GKtzJe-VcxSHuFr_Ag130_assertion { miriam-gene:25 a ncit:C16612 . lld:C0023473 a ncit:C7057 . dgn-gda:DGN20d13a3debcb7b8b8a87dfc37b869d79 sio:SIO_000628 miriam-gene:25, lld:C0023473; a sio:SIO_001121 . } dgn-np:NP1409217.RAg4u3HW-pCF-OWL46PKVcl7mB0GKtzJe-VcxSHuFr_Ag130_provenance { dgn-np:NP1409217.RAg4u3HW-pCF-OWL46PKVcl7mB0GKtzJe-VcxSHuFr_Ag130_assertion dcterms:description "[We arrived at the following conclusions: (1) dual-color FISH enables an accurate detection and monitoring of the size of the Ph-positive clone in CML at diagnosis and after IFN-therapy; (2) FISH is more accurate than CCA, especially at low levels of Ph-positive cells; (3) testing of directly harvested BM samples is feasible and accurate, giving the opportunity to perform centralized FISH analysis in the context of multicentre trials; (4) the percentage of BCR/ABL+ PB cells usually, though not invariably, reflects the frequency of mutated cells in the BM.]. 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:9823946; 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:NP1409217.RAg4u3HW-pCF-OWL46PKVcl7mB0GKtzJe-VcxSHuFr_Ag130_publicationInfo { this: dcterms:created "2016-05-13T12:52:25+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" . }