@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:NP242930.RAT2uotBY1XOZosfJQBQw5luipa14FSBu7XQNZJ509EW8130_head { this: np:hasAssertion dgn-np:NP242930.RAT2uotBY1XOZosfJQBQw5luipa14FSBu7XQNZJ509EW8130_assertion; np:hasProvenance dgn-np:NP242930.RAT2uotBY1XOZosfJQBQw5luipa14FSBu7XQNZJ509EW8130_provenance; np:hasPublicationInfo dgn-np:NP242930.RAT2uotBY1XOZosfJQBQw5luipa14FSBu7XQNZJ509EW8130_publicationInfo; a np:Nanopublication . dgn-np:NP242930.RAT2uotBY1XOZosfJQBQw5luipa14FSBu7XQNZJ509EW8130_assertion a np:Assertion . dgn-np:NP242930.RAT2uotBY1XOZosfJQBQw5luipa14FSBu7XQNZJ509EW8130_provenance a np:Provenance . dgn-np:NP242930.RAT2uotBY1XOZosfJQBQw5luipa14FSBu7XQNZJ509EW8130_publicationInfo a np:PublicationInfo . } dgn-np:NP242930.RAT2uotBY1XOZosfJQBQw5luipa14FSBu7XQNZJ509EW8130_assertion { miriam-gene:3717 a ncit:C16612 . lld:C0013080 a ncit:C7057 . dgn-gda:DGNb6cf704dcb4db436318b166b724e04e9 sio:SIO_000628 miriam-gene:3717, lld:C0013080; a sio:SIO_001122 . } dgn-np:NP242930.RAT2uotBY1XOZosfJQBQw5luipa14FSBu7XQNZJ509EW8130_provenance { dgn-np:NP242930.RAT2uotBY1XOZosfJQBQw5luipa14FSBu7XQNZJ509EW8130_assertion dcterms:description "[a complex molecular pathogenesis for Down syndrome and acute lymphoblastic leukemia leukemogenesis, with trisomy 21 as an initiating factor and with chromosome aneuploidy, gene deletions, and activating JAK2 mutations as complementary genetic events ]. 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:18927438; 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:NP242930.RAT2uotBY1XOZosfJQBQw5luipa14FSBu7XQNZJ509EW8130_publicationInfo { this: dcterms:created "2016-05-13T12:43:36+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" . }