@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:NP385084.RAOHK2sqGCm1xTV37iJSI5HzJovKbgcu12Fhf-cQNNUvY130_head { this: np:hasAssertion dgn-np:NP385084.RAOHK2sqGCm1xTV37iJSI5HzJovKbgcu12Fhf-cQNNUvY130_assertion; np:hasProvenance dgn-np:NP385084.RAOHK2sqGCm1xTV37iJSI5HzJovKbgcu12Fhf-cQNNUvY130_provenance; np:hasPublicationInfo dgn-np:NP385084.RAOHK2sqGCm1xTV37iJSI5HzJovKbgcu12Fhf-cQNNUvY130_publicationInfo; a np:Nanopublication . dgn-np:NP385084.RAOHK2sqGCm1xTV37iJSI5HzJovKbgcu12Fhf-cQNNUvY130_assertion a np:Assertion . dgn-np:NP385084.RAOHK2sqGCm1xTV37iJSI5HzJovKbgcu12Fhf-cQNNUvY130_provenance a np:Provenance . dgn-np:NP385084.RAOHK2sqGCm1xTV37iJSI5HzJovKbgcu12Fhf-cQNNUvY130_publicationInfo a np:PublicationInfo . } dgn-np:NP385084.RAOHK2sqGCm1xTV37iJSI5HzJovKbgcu12Fhf-cQNNUvY130_assertion { miriam-gene:6774 a ncit:C16612 . lld:C0376358 a ncit:C7057 . dgn-gda:DGN3ba0a6a37ede5114cec37be485e0ab2d sio:SIO_000628 miriam-gene:6774, lld:C0376358; a sio:SIO_001121 . } dgn-np:NP385084.RAOHK2sqGCm1xTV37iJSI5HzJovKbgcu12Fhf-cQNNUvY130_provenance { dgn-np:NP385084.RAOHK2sqGCm1xTV37iJSI5HzJovKbgcu12Fhf-cQNNUvY130_assertion dcterms:description "[Screening of the prostate cancer cell lines LNCaP, PC3 and DU145 allowed the mapping of specific regions where genome copy number appeared altered and led to the identification of two novel regions of complete loss at 17q21.31 (500 kb spanning STAT3) and at 10q23.1 (50-350 kb spanning SFTPA2) in the PC3 cell line.]. 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:12606952; 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:NP385084.RAOHK2sqGCm1xTV37iJSI5HzJovKbgcu12Fhf-cQNNUvY130_publicationInfo { this: dcterms:created "2016-05-13T12:44:39+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" . }