@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:NP241298.RAnD-0HDQ2lthFMf86jmPksZqDWRbT8rWKkYC03X6_dt8130_head { this: np:hasAssertion dgn-np:NP241298.RAnD-0HDQ2lthFMf86jmPksZqDWRbT8rWKkYC03X6_dt8130_assertion; np:hasProvenance dgn-np:NP241298.RAnD-0HDQ2lthFMf86jmPksZqDWRbT8rWKkYC03X6_dt8130_provenance; np:hasPublicationInfo dgn-np:NP241298.RAnD-0HDQ2lthFMf86jmPksZqDWRbT8rWKkYC03X6_dt8130_publicationInfo; a np:Nanopublication . dgn-np:NP241298.RAnD-0HDQ2lthFMf86jmPksZqDWRbT8rWKkYC03X6_dt8130_assertion a np:Assertion . dgn-np:NP241298.RAnD-0HDQ2lthFMf86jmPksZqDWRbT8rWKkYC03X6_dt8130_provenance a np:Provenance . dgn-np:NP241298.RAnD-0HDQ2lthFMf86jmPksZqDWRbT8rWKkYC03X6_dt8130_publicationInfo a np:PublicationInfo . } dgn-np:NP241298.RAnD-0HDQ2lthFMf86jmPksZqDWRbT8rWKkYC03X6_dt8130_assertion { miriam-gene:3717 a ncit:C16612 . lld:C0032463 a ncit:C7057 . dgn-gda:DGNcf1351fcb297a48bf7c4f8358ec7fa44 sio:SIO_000628 miriam-gene:3717, lld:C0032463; a sio:SIO_001122 . } dgn-np:NP241298.RAnD-0HDQ2lthFMf86jmPksZqDWRbT8rWKkYC03X6_dt8130_provenance { dgn-np:NP241298.RAnD-0HDQ2lthFMf86jmPksZqDWRbT8rWKkYC03X6_dt8130_assertion dcterms:description "[JAK2 V617F mutation was detected in 124/158 chronic myeloproliferative disease patients; 90.2, 72.1, 63.2 & 50% of polycythemia vera, essential thrombocythemia, idiopathic myelofibrosis & unclassified (U) -MPD cases, respectively, showed the mutation ]. 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:18720212; prov:wasDerivedFrom dgn-void:lhgdn-20090331; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:lhgdn-20090331 pav:importedOn "2009-03-31"^^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:NP241298.RAnD-0HDQ2lthFMf86jmPksZqDWRbT8rWKkYC03X6_dt8130_publicationInfo { this: dcterms:created "2016-05-13T12:43:35+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" . }