@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:NP797047.RAGOWyAnxRreGrYaRPtPnkJ8zdYcTaw57Qgl7Wcx58qi8130_head { this: np:hasAssertion dgn-np:NP797047.RAGOWyAnxRreGrYaRPtPnkJ8zdYcTaw57Qgl7Wcx58qi8130_assertion; np:hasProvenance dgn-np:NP797047.RAGOWyAnxRreGrYaRPtPnkJ8zdYcTaw57Qgl7Wcx58qi8130_provenance; np:hasPublicationInfo dgn-np:NP797047.RAGOWyAnxRreGrYaRPtPnkJ8zdYcTaw57Qgl7Wcx58qi8130_publicationInfo; a np:Nanopublication . dgn-np:NP797047.RAGOWyAnxRreGrYaRPtPnkJ8zdYcTaw57Qgl7Wcx58qi8130_assertion a np:Assertion . dgn-np:NP797047.RAGOWyAnxRreGrYaRPtPnkJ8zdYcTaw57Qgl7Wcx58qi8130_provenance a np:Provenance . dgn-np:NP797047.RAGOWyAnxRreGrYaRPtPnkJ8zdYcTaw57Qgl7Wcx58qi8130_publicationInfo a np:PublicationInfo . } dgn-np:NP797047.RAGOWyAnxRreGrYaRPtPnkJ8zdYcTaw57Qgl7Wcx58qi8130_assertion { miriam-gene:8493 a ncit:C16612 . lld:C0242621 a ncit:C7057 . dgn-gda:DGNbaf81d61541f0dffcf018fdb69f89b8d sio:SIO_000628 miriam-gene:8493, lld:C0242621; a sio:SIO_001121 . } dgn-np:NP797047.RAGOWyAnxRreGrYaRPtPnkJ8zdYcTaw57Qgl7Wcx58qi8130_provenance { dgn-np:NP797047.RAGOWyAnxRreGrYaRPtPnkJ8zdYcTaw57Qgl7Wcx58qi8130_assertion dcterms:description "[We examined primary medulloblastoma specimens and cell lines, and detected WIP1 copy gain and amplification prevalent among but not exclusively in the tumors with 17q gain and isochromosome 17q (i17q), which are among the most common cytogenetic lesions in medulloblastoma.]. 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:17932621; prov:wasDerivedFrom dgn-void:befree-20150227; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP797047.RAGOWyAnxRreGrYaRPtPnkJ8zdYcTaw57Qgl7Wcx58qi8130_publicationInfo { this: dcterms:created "2015-08-25T14:45:42+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 "v3.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v3.0.0" . }