@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:NP930076.RAW-PggFTGRxEWqQ0YDs8xP317dkLxSH0duNmAMGGHiCg130_head { this: np:hasAssertion dgn-np:NP930076.RAW-PggFTGRxEWqQ0YDs8xP317dkLxSH0duNmAMGGHiCg130_assertion; np:hasProvenance dgn-np:NP930076.RAW-PggFTGRxEWqQ0YDs8xP317dkLxSH0duNmAMGGHiCg130_provenance; np:hasPublicationInfo dgn-np:NP930076.RAW-PggFTGRxEWqQ0YDs8xP317dkLxSH0duNmAMGGHiCg130_publicationInfo; a np:Nanopublication . dgn-np:NP930076.RAW-PggFTGRxEWqQ0YDs8xP317dkLxSH0duNmAMGGHiCg130_assertion a np:Assertion . dgn-np:NP930076.RAW-PggFTGRxEWqQ0YDs8xP317dkLxSH0duNmAMGGHiCg130_provenance a np:Provenance . dgn-np:NP930076.RAW-PggFTGRxEWqQ0YDs8xP317dkLxSH0duNmAMGGHiCg130_publicationInfo a np:PublicationInfo . } dgn-np:NP930076.RAW-PggFTGRxEWqQ0YDs8xP317dkLxSH0duNmAMGGHiCg130_assertion { miriam-gene:7157 a ncit:C16612 . lld:C0206716 a ncit:C7057 . dgn-gda:DGN8cb1d854d0a73831f75c4e47b9ffa637 sio:SIO_000628 miriam-gene:7157, lld:C0206716; a sio:SIO_001121 . } dgn-np:NP930076.RAW-PggFTGRxEWqQ0YDs8xP317dkLxSH0duNmAMGGHiCg130_provenance { dgn-np:NP930076.RAW-PggFTGRxEWqQ0YDs8xP317dkLxSH0duNmAMGGHiCg130_assertion dcterms:description "[The present case is unusual in four aspects: (i) it arose from a low-grade ganglioglioma in the absence of previous radiation or chemotherapy, which is the fourth reported case; (ii) the original tumor showed a high proliferative index on flow cytometry but a low Ki-67 labeling index, implying that the application of flow cytometry might play a certain role in predicting biological and clinical behavior of low grade gangliogliomas; (iii) p53 mutation and deletion appeared in the secondary glioblastoma, which was not shown in the original well-differentiated ganglioglioma; and (iv) the transformed glioblastoma showed p16 inactivation detected by methylation and deletion, which are relatively uncommon genetic events in secondary glioblastomas.]. 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:14629754; prov:wasDerivedFrom dgn-void:befree-20140225; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP930076.RAW-PggFTGRxEWqQ0YDs8xP317dkLxSH0duNmAMGGHiCg130_publicationInfo { this: dcterms:created "2014-10-02T12:41:30+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetrdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v2.1.0.0" . dgn-void:disgenetrdf pav:version "v2.1.0" . }