@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:NP413550.RAJnHGZ20MngGuS58t5-RKrXg12z-5-F7l2WQKIWIOoRY130_head { this: np:hasAssertion dgn-np:NP413550.RAJnHGZ20MngGuS58t5-RKrXg12z-5-F7l2WQKIWIOoRY130_assertion; np:hasProvenance dgn-np:NP413550.RAJnHGZ20MngGuS58t5-RKrXg12z-5-F7l2WQKIWIOoRY130_provenance; np:hasPublicationInfo dgn-np:NP413550.RAJnHGZ20MngGuS58t5-RKrXg12z-5-F7l2WQKIWIOoRY130_publicationInfo; a np:Nanopublication . dgn-np:NP413550.RAJnHGZ20MngGuS58t5-RKrXg12z-5-F7l2WQKIWIOoRY130_assertion a np:Assertion . dgn-np:NP413550.RAJnHGZ20MngGuS58t5-RKrXg12z-5-F7l2WQKIWIOoRY130_provenance a np:Provenance . dgn-np:NP413550.RAJnHGZ20MngGuS58t5-RKrXg12z-5-F7l2WQKIWIOoRY130_publicationInfo a np:PublicationInfo . } dgn-np:NP413550.RAJnHGZ20MngGuS58t5-RKrXg12z-5-F7l2WQKIWIOoRY130_assertion { miriam-gene:613 a ncit:C16612 . lld:C0023418 a ncit:C7057 . dgn-gda:DGN93b241c7e9dd072642e9c02bc577ec9a sio:SIO_000628 miriam-gene:613, lld:C0023418; a sio:SIO_001121 . } dgn-np:NP413550.RAJnHGZ20MngGuS58t5-RKrXg12z-5-F7l2WQKIWIOoRY130_provenance { dgn-np:NP413550.RAJnHGZ20MngGuS58t5-RKrXg12z-5-F7l2WQKIWIOoRY130_assertion dcterms:description "[The cloning of specific chromosomal breakpoints identified in leukemia (as has been done for CML) will result in specific probes which can be used to make the diagnosis rapidly at the molecular level.]. 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:1434816; 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:NP413550.RAJnHGZ20MngGuS58t5-RKrXg12z-5-F7l2WQKIWIOoRY130_publicationInfo { this: dcterms:created "2016-05-13T12:44:52+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" . }