@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:NP627341.RAP43ScILVlCtGQLGMGkDiZE26Z1DlkVOp8g7yklRm8u4130_head { this: np:hasAssertion dgn-np:NP627341.RAP43ScILVlCtGQLGMGkDiZE26Z1DlkVOp8g7yklRm8u4130_assertion; np:hasProvenance dgn-np:NP627341.RAP43ScILVlCtGQLGMGkDiZE26Z1DlkVOp8g7yklRm8u4130_provenance; np:hasPublicationInfo dgn-np:NP627341.RAP43ScILVlCtGQLGMGkDiZE26Z1DlkVOp8g7yklRm8u4130_publicationInfo; a np:Nanopublication . dgn-np:NP627341.RAP43ScILVlCtGQLGMGkDiZE26Z1DlkVOp8g7yklRm8u4130_assertion a np:Assertion . dgn-np:NP627341.RAP43ScILVlCtGQLGMGkDiZE26Z1DlkVOp8g7yklRm8u4130_provenance a np:Provenance . dgn-np:NP627341.RAP43ScILVlCtGQLGMGkDiZE26Z1DlkVOp8g7yklRm8u4130_publicationInfo a np:PublicationInfo . } dgn-np:NP627341.RAP43ScILVlCtGQLGMGkDiZE26Z1DlkVOp8g7yklRm8u4130_assertion { miriam-gene:5315 a ncit:C16612 . lld:C1306459 a ncit:C7057 . dgn-gda:DGNd47d25a6e335a0f5643d1506aa3e57fc sio:SIO_000628 miriam-gene:5315, lld:C1306459; a sio:SIO_001121 . } dgn-np:NP627341.RAP43ScILVlCtGQLGMGkDiZE26Z1DlkVOp8g7yklRm8u4130_provenance { dgn-np:NP627341.RAP43ScILVlCtGQLGMGkDiZE26Z1DlkVOp8g7yklRm8u4130_assertion dcterms:description "[Such a dominant negative impaired function of PKM2 in tumor development is not known; this study demonstrates for the first time the possible predisposition of Bloom syndrome patients with impaired PKM2 activity to cancer and the importance of studying genetic variations in PKM2 in the future to understand their relevance in cancer in general.]. 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:24492614; 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:NP627341.RAP43ScILVlCtGQLGMGkDiZE26Z1DlkVOp8g7yklRm8u4130_publicationInfo { this: dcterms:created "2015-08-25T14:43:55+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" . }