@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:NP1079234.RAYsdVsRByDdipMgCs1bbRuo9ajCjlo6kWp7RQ9ZZOnRk130_head { this: np:hasAssertion dgn-np:NP1079234.RAYsdVsRByDdipMgCs1bbRuo9ajCjlo6kWp7RQ9ZZOnRk130_assertion; np:hasProvenance dgn-np:NP1079234.RAYsdVsRByDdipMgCs1bbRuo9ajCjlo6kWp7RQ9ZZOnRk130_provenance; np:hasPublicationInfo dgn-np:NP1079234.RAYsdVsRByDdipMgCs1bbRuo9ajCjlo6kWp7RQ9ZZOnRk130_publicationInfo; a np:Nanopublication . dgn-np:NP1079234.RAYsdVsRByDdipMgCs1bbRuo9ajCjlo6kWp7RQ9ZZOnRk130_assertion a np:Assertion . dgn-np:NP1079234.RAYsdVsRByDdipMgCs1bbRuo9ajCjlo6kWp7RQ9ZZOnRk130_provenance a np:Provenance . dgn-np:NP1079234.RAYsdVsRByDdipMgCs1bbRuo9ajCjlo6kWp7RQ9ZZOnRk130_publicationInfo a np:PublicationInfo . } dgn-np:NP1079234.RAYsdVsRByDdipMgCs1bbRuo9ajCjlo6kWp7RQ9ZZOnRk130_assertion { miriam-gene:171023 a ncit:C16612 . lld:C0023480 a ncit:C7057 . dgn-gda:DGNd83a335134c3fe4e2ac70a7b7ab0fd26 sio:SIO_000628 miriam-gene:171023, lld:C0023480; a sio:SIO_001121 . } dgn-np:NP1079234.RAYsdVsRByDdipMgCs1bbRuo9ajCjlo6kWp7RQ9ZZOnRk130_provenance { dgn-np:NP1079234.RAYsdVsRByDdipMgCs1bbRuo9ajCjlo6kWp7RQ9ZZOnRk130_assertion dcterms:description "[We genotyped ASXL1 and up to 18 other genes including epigenetic (TET2, EZH2, IDH1, IDH2, DNMT3A), splicing (SF3B1, SRSF2, ZRSF2, U2AF1), transcription (RUNX1, NPM1, TP53), and signaling (NRAS, KRAS, CBL, JAK2, FLT3) regulators in 312 patients with CMML.]. 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:23690417; 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:NP1079234.RAYsdVsRByDdipMgCs1bbRuo9ajCjlo6kWp7RQ9ZZOnRk130_publicationInfo { this: dcterms:created "2016-05-13T12:49:55+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" . }