@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:NP219626.RAjegDkWRDz6fWjFWPuWIqTkfIxIo-DYKSO81cYEXagQM130_head { this: np:hasAssertion dgn-np:NP219626.RAjegDkWRDz6fWjFWPuWIqTkfIxIo-DYKSO81cYEXagQM130_assertion; np:hasProvenance dgn-np:NP219626.RAjegDkWRDz6fWjFWPuWIqTkfIxIo-DYKSO81cYEXagQM130_provenance; np:hasPublicationInfo dgn-np:NP219626.RAjegDkWRDz6fWjFWPuWIqTkfIxIo-DYKSO81cYEXagQM130_publicationInfo; a np:Nanopublication . dgn-np:NP219626.RAjegDkWRDz6fWjFWPuWIqTkfIxIo-DYKSO81cYEXagQM130_assertion a np:Assertion . dgn-np:NP219626.RAjegDkWRDz6fWjFWPuWIqTkfIxIo-DYKSO81cYEXagQM130_provenance a np:Provenance . dgn-np:NP219626.RAjegDkWRDz6fWjFWPuWIqTkfIxIo-DYKSO81cYEXagQM130_publicationInfo a np:PublicationInfo . } dgn-np:NP219626.RAjegDkWRDz6fWjFWPuWIqTkfIxIo-DYKSO81cYEXagQM130_assertion { miriam-gene:25 a ncit:C16612 . lld:C1840451 a ncit:C7057 . dgn-gda:DGN1428fe9f3e9ee25d746871540ec32ed1 sio:SIO_000628 miriam-gene:25, lld:C1840451; a sio:SIO_001121 . } dgn-np:NP219626.RAjegDkWRDz6fWjFWPuWIqTkfIxIo-DYKSO81cYEXagQM130_provenance { dgn-np:NP219626.RAjegDkWRDz6fWjFWPuWIqTkfIxIo-DYKSO81cYEXagQM130_assertion dcterms:description "[The rare e14a3 (b3a3) fusion of the BCR ABL gene is present in Indian population as demonstrated from this first report and clinical laboratories using commercial kit that do not cover such rare fusions are likely to generate false result thereby declaring complete molecular remission in CML patients under therapy while conducting MRD assay using RT-PCR technology.]. 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:24072036; 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:NP219626.RAjegDkWRDz6fWjFWPuWIqTkfIxIo-DYKSO81cYEXagQM130_publicationInfo { this: dcterms:created "2015-08-25T14:39:45+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" . }