@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:NP980154.RATGP9LBWfWBxG9nP3lA2FxO6aBEUoKpRQa-AMmnh2Bik130_head { this: np:hasAssertion dgn-np:NP980154.RATGP9LBWfWBxG9nP3lA2FxO6aBEUoKpRQa-AMmnh2Bik130_assertion; np:hasProvenance dgn-np:NP980154.RATGP9LBWfWBxG9nP3lA2FxO6aBEUoKpRQa-AMmnh2Bik130_provenance; np:hasPublicationInfo dgn-np:NP980154.RATGP9LBWfWBxG9nP3lA2FxO6aBEUoKpRQa-AMmnh2Bik130_publicationInfo; a np:Nanopublication . dgn-np:NP980154.RATGP9LBWfWBxG9nP3lA2FxO6aBEUoKpRQa-AMmnh2Bik130_assertion a np:Assertion . dgn-np:NP980154.RATGP9LBWfWBxG9nP3lA2FxO6aBEUoKpRQa-AMmnh2Bik130_provenance a np:Provenance . dgn-np:NP980154.RATGP9LBWfWBxG9nP3lA2FxO6aBEUoKpRQa-AMmnh2Bik130_publicationInfo a np:PublicationInfo . } dgn-np:NP980154.RATGP9LBWfWBxG9nP3lA2FxO6aBEUoKpRQa-AMmnh2Bik130_assertion { miriam-gene:7157 a ncit:C16612 . lld:C0677886 a ncit:C7057 . dgn-gda:DGN41f232074ab76189cb65adff17a0e4d0 sio:SIO_000628 miriam-gene:7157, lld:C0677886; a sio:SIO_001121 . } dgn-np:NP980154.RATGP9LBWfWBxG9nP3lA2FxO6aBEUoKpRQa-AMmnh2Bik130_provenance { dgn-np:NP980154.RATGP9LBWfWBxG9nP3lA2FxO6aBEUoKpRQa-AMmnh2Bik130_assertion dcterms:description "[Human ovarian carcinoma cell lines SKOV3 and multidrug resistant phenotype SKVCR cells were used and wild-type p53 (wt p53) and mutant 175H constructs were introduced into cells to establish cell models with different p53 status by gene engineering, the sensitivity to vincristine (VCR), cisplatin (DDP), pirarubicin (THP) and etoposide (VP-16) were detected by MTT assay, Western blot and quantitative real-time PCR were used to detect the expression of protein and mRNA, especially, monodansylcadaverine (MDC) staining was used for autophagy rate, Hoechst 33342/propidium iodide (PI) were used to assess apoptosis and necrosis.]. 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:22564245; 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:NP980154.RATGP9LBWfWBxG9nP3lA2FxO6aBEUoKpRQa-AMmnh2Bik130_publicationInfo { this: dcterms:created "2016-05-13T12:49:09+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" . }