@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:NP635492.RAQwZd6eQ9p-Nrk1w4o_A7EFMsHKolD9K4RNMyA9wIQTM130_head { this: np:hasAssertion dgn-np:NP635492.RAQwZd6eQ9p-Nrk1w4o_A7EFMsHKolD9K4RNMyA9wIQTM130_assertion; np:hasProvenance dgn-np:NP635492.RAQwZd6eQ9p-Nrk1w4o_A7EFMsHKolD9K4RNMyA9wIQTM130_provenance; np:hasPublicationInfo dgn-np:NP635492.RAQwZd6eQ9p-Nrk1w4o_A7EFMsHKolD9K4RNMyA9wIQTM130_publicationInfo; a np:Nanopublication . dgn-np:NP635492.RAQwZd6eQ9p-Nrk1w4o_A7EFMsHKolD9K4RNMyA9wIQTM130_assertion a np:Assertion . dgn-np:NP635492.RAQwZd6eQ9p-Nrk1w4o_A7EFMsHKolD9K4RNMyA9wIQTM130_provenance a np:Provenance . dgn-np:NP635492.RAQwZd6eQ9p-Nrk1w4o_A7EFMsHKolD9K4RNMyA9wIQTM130_publicationInfo a np:PublicationInfo . } dgn-np:NP635492.RAQwZd6eQ9p-Nrk1w4o_A7EFMsHKolD9K4RNMyA9wIQTM130_assertion { miriam-gene:25 a ncit:C16612 . lld:C1292778 a ncit:C7057 . dgn-gda:DGNf13ae68d156cfacb3cc461cdfb2d3825 sio:SIO_000628 miriam-gene:25, lld:C1292778; a sio:SIO_001121 . } dgn-np:NP635492.RAQwZd6eQ9p-Nrk1w4o_A7EFMsHKolD9K4RNMyA9wIQTM130_provenance { dgn-np:NP635492.RAQwZd6eQ9p-Nrk1w4o_A7EFMsHKolD9K4RNMyA9wIQTM130_assertion dcterms:description "[Recent years showed significant progress in the molecular characterization of the chronic myeloproliferative disorders (CMPD) which are classified according to the WHO classification of 2001 as polycythemia vera (PV), chronic idiopathic myelofibrosis (CIMF), essential thrombocythemia (ET), CMPD/unclassifiable (CMPD-U), chronic neutrophilic leukemia, and chronic eosinophilic leukemia (CEL)/hypereosinophilic syndrome, all to be delineated from BCR/ABL-positive chronic myeloid leukemia (CML).]. 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:17938925; 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:NP635492.RAQwZd6eQ9p-Nrk1w4o_A7EFMsHKolD9K4RNMyA9wIQTM130_publicationInfo { this: dcterms:created "2016-05-13T12:46:33+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" . }