@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:NP298760.RAvjjprTY5n7XnnN7OCjWtgXxg1PyJUEO-DeA5CJ56gcY130_head { this: np:hasAssertion dgn-np:NP298760.RAvjjprTY5n7XnnN7OCjWtgXxg1PyJUEO-DeA5CJ56gcY130_assertion; np:hasProvenance dgn-np:NP298760.RAvjjprTY5n7XnnN7OCjWtgXxg1PyJUEO-DeA5CJ56gcY130_provenance; np:hasPublicationInfo dgn-np:NP298760.RAvjjprTY5n7XnnN7OCjWtgXxg1PyJUEO-DeA5CJ56gcY130_publicationInfo; a np:Nanopublication . dgn-np:NP298760.RAvjjprTY5n7XnnN7OCjWtgXxg1PyJUEO-DeA5CJ56gcY130_assertion a np:Assertion . dgn-np:NP298760.RAvjjprTY5n7XnnN7OCjWtgXxg1PyJUEO-DeA5CJ56gcY130_provenance a np:Provenance . dgn-np:NP298760.RAvjjprTY5n7XnnN7OCjWtgXxg1PyJUEO-DeA5CJ56gcY130_publicationInfo a np:PublicationInfo . } dgn-np:NP298760.RAvjjprTY5n7XnnN7OCjWtgXxg1PyJUEO-DeA5CJ56gcY130_assertion { miriam-gene:991 a ncit:C16612 . lld:C2239176 a ncit:C7057 . dgn-gda:DGNb658caa798f55620b9d9014b5cdebeef sio:SIO_000628 miriam-gene:991, lld:C2239176; a sio:SIO_001121 . } dgn-np:NP298760.RAvjjprTY5n7XnnN7OCjWtgXxg1PyJUEO-DeA5CJ56gcY130_provenance { dgn-np:NP298760.RAvjjprTY5n7XnnN7OCjWtgXxg1PyJUEO-DeA5CJ56gcY130_assertion dcterms:description "[While some polymorphic base changes were noted in BUB1, BUBR1, and CDC20, no mutations responsible for impairment of the mitotic checkpoint were found in either the HCC cell lines or HCC specimens, which suggests that these genes did not seem to be involved in tumor development in HCC.]. 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:11932908; 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:NP298760.RAvjjprTY5n7XnnN7OCjWtgXxg1PyJUEO-DeA5CJ56gcY130_publicationInfo { this: dcterms:created "2015-08-25T14:40:31+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" . }