@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:NP1018522.RAkXW_xk7mFnTyH3-U1yEks4OE80Y4Q2RNeKqDU7Chni0130_head { this: np:hasAssertion dgn-np:NP1018522.RAkXW_xk7mFnTyH3-U1yEks4OE80Y4Q2RNeKqDU7Chni0130_assertion ; np:hasProvenance dgn-np:NP1018522.RAkXW_xk7mFnTyH3-U1yEks4OE80Y4Q2RNeKqDU7Chni0130_provenance ; np:hasPublicationInfo dgn-np:NP1018522.RAkXW_xk7mFnTyH3-U1yEks4OE80Y4Q2RNeKqDU7Chni0130_publicationInfo ; a np:Nanopublication . dgn-np:NP1018522.RAkXW_xk7mFnTyH3-U1yEks4OE80Y4Q2RNeKqDU7Chni0130_assertion a np:Assertion . dgn-np:NP1018522.RAkXW_xk7mFnTyH3-U1yEks4OE80Y4Q2RNeKqDU7Chni0130_provenance a np:Provenance . dgn-np:NP1018522.RAkXW_xk7mFnTyH3-U1yEks4OE80Y4Q2RNeKqDU7Chni0130_publicationInfo a np:PublicationInfo . } dgn-np:NP1018522.RAkXW_xk7mFnTyH3-U1yEks4OE80Y4Q2RNeKqDU7Chni0130_assertion { miriam-gene:102724594 a ncit:C16612 . lld:C0346429 a ncit:C7057 . dgn-gda:DGNbfbe5d0ac75d5328d55c7ca3b9a53c6f sio:SIO_000628 miriam-gene:102724594 , lld:C0346429 ; a sio:SIO_001121 . } dgn-np:NP1018522.RAkXW_xk7mFnTyH3-U1yEks4OE80Y4Q2RNeKqDU7Chni0130_provenance { dgn-np:NP1018522.RAkXW_xk7mFnTyH3-U1yEks4OE80Y4Q2RNeKqDU7Chni0130_assertion dcterms:description "[Although recurrent somatic mutations in the splicing factor U2AF1 (also known as U2AF35) have been identified in multiple cancer types, the effects of these mutations on the cancer transcriptome have yet to be fully elucidated.]. 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:24498085 ; 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:NP1018522.RAkXW_xk7mFnTyH3-U1yEks4OE80Y4Q2RNeKqDU7Chni0130_publicationInfo { this: dcterms:created "2015-08-25T14:48:12+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" . }