@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:NP822406.RAusvKUp9BnDgDD9e72HHrkqdTMjpzPygtJUXQli2KvJg130_head { this: np:hasAssertion dgn-np:NP822406.RAusvKUp9BnDgDD9e72HHrkqdTMjpzPygtJUXQli2KvJg130_assertion; np:hasProvenance dgn-np:NP822406.RAusvKUp9BnDgDD9e72HHrkqdTMjpzPygtJUXQli2KvJg130_provenance; np:hasPublicationInfo dgn-np:NP822406.RAusvKUp9BnDgDD9e72HHrkqdTMjpzPygtJUXQli2KvJg130_publicationInfo; a np:Nanopublication . dgn-np:NP822406.RAusvKUp9BnDgDD9e72HHrkqdTMjpzPygtJUXQli2KvJg130_assertion a np:Assertion . dgn-np:NP822406.RAusvKUp9BnDgDD9e72HHrkqdTMjpzPygtJUXQli2KvJg130_provenance a np:Provenance . dgn-np:NP822406.RAusvKUp9BnDgDD9e72HHrkqdTMjpzPygtJUXQli2KvJg130_publicationInfo a np:PublicationInfo . } dgn-np:NP822406.RAusvKUp9BnDgDD9e72HHrkqdTMjpzPygtJUXQli2KvJg130_assertion { miriam-gene:9401 a ncit:C16612 . lld:C0006826 a ncit:C7057 . dgn-gda:DGNbfab31915e43ac67b15f186feac1481a sio:SIO_000628 miriam-gene:9401, lld:C0006826; a sio:SIO_001121 . } dgn-np:NP822406.RAusvKUp9BnDgDD9e72HHrkqdTMjpzPygtJUXQli2KvJg130_provenance { dgn-np:NP822406.RAusvKUp9BnDgDD9e72HHrkqdTMjpzPygtJUXQli2KvJg130_assertion dcterms:description "[Although loss of RecQL4 function due to gene mutations causally linked to occurrence of human RTS with features of premature aging and cancer predisposition, our studies provide the evidence that overexpression of RecQL4 due to gene amplification play a critical role in human breast tumor progression.]. 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:23894508; 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:NP822406.RAusvKUp9BnDgDD9e72HHrkqdTMjpzPygtJUXQli2KvJg130_publicationInfo { this: dcterms:created "2015-08-25T14:45:58+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" . }