@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:NP1149729.RArIXTfErzwWAeUKwf4dzzWOdrMwwxgnECkFrJEbjbogM130_head { this: np:hasAssertion dgn-np:NP1149729.RArIXTfErzwWAeUKwf4dzzWOdrMwwxgnECkFrJEbjbogM130_assertion; np:hasProvenance dgn-np:NP1149729.RArIXTfErzwWAeUKwf4dzzWOdrMwwxgnECkFrJEbjbogM130_provenance; np:hasPublicationInfo dgn-np:NP1149729.RArIXTfErzwWAeUKwf4dzzWOdrMwwxgnECkFrJEbjbogM130_publicationInfo; a np:Nanopublication . dgn-np:NP1149729.RArIXTfErzwWAeUKwf4dzzWOdrMwwxgnECkFrJEbjbogM130_assertion a np:Assertion . dgn-np:NP1149729.RArIXTfErzwWAeUKwf4dzzWOdrMwwxgnECkFrJEbjbogM130_provenance a np:Provenance . dgn-np:NP1149729.RArIXTfErzwWAeUKwf4dzzWOdrMwwxgnECkFrJEbjbogM130_publicationInfo a np:PublicationInfo . } dgn-np:NP1149729.RArIXTfErzwWAeUKwf4dzzWOdrMwwxgnECkFrJEbjbogM130_assertion { miriam-gene:5426 a ncit:C16612 . lld:C0476089 a ncit:C7057 . dgn-gda:DGN0b8acaae4a604ca07dfc020cdde493b3 sio:SIO_000628 miriam-gene:5426, lld:C0476089; a sio:SIO_001122 . } dgn-np:NP1149729.RArIXTfErzwWAeUKwf4dzzWOdrMwwxgnECkFrJEbjbogM130_provenance { dgn-np:NP1149729.RArIXTfErzwWAeUKwf4dzzWOdrMwwxgnECkFrJEbjbogM130_assertion dcterms:description "[Recently, POLE1 mutations were detected frequently in colorectal and endometrial carcinomas while with lower frequency in several other types of cancer, and the p.P286R and p.V411L mutations were the potential mutation hotspots in human cancers.]. 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:24472300; 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:NP1149729.RArIXTfErzwWAeUKwf4dzzWOdrMwwxgnECkFrJEbjbogM130_publicationInfo { this: dcterms:created "2016-05-13T12:50:27+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" . }