@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:NP782233.RANxac75KC5wmnyHpegDkncMsctW9QhRpO2EDMy5V3iIo130_head { this: np:hasAssertion dgn-np:NP782233.RANxac75KC5wmnyHpegDkncMsctW9QhRpO2EDMy5V3iIo130_assertion; np:hasProvenance dgn-np:NP782233.RANxac75KC5wmnyHpegDkncMsctW9QhRpO2EDMy5V3iIo130_provenance; np:hasPublicationInfo dgn-np:NP782233.RANxac75KC5wmnyHpegDkncMsctW9QhRpO2EDMy5V3iIo130_publicationInfo; a np:Nanopublication . dgn-np:NP782233.RANxac75KC5wmnyHpegDkncMsctW9QhRpO2EDMy5V3iIo130_assertion a np:Assertion . dgn-np:NP782233.RANxac75KC5wmnyHpegDkncMsctW9QhRpO2EDMy5V3iIo130_provenance a np:Provenance . dgn-np:NP782233.RANxac75KC5wmnyHpegDkncMsctW9QhRpO2EDMy5V3iIo130_publicationInfo a np:PublicationInfo . } dgn-np:NP782233.RANxac75KC5wmnyHpegDkncMsctW9QhRpO2EDMy5V3iIo130_assertion { miriam-gene:3077 a ncit:C16612 . lld:C0018995 a ncit:C7057 . dgn-gda:DGN601a92d206e595123ad97c9666d50284 sio:SIO_000628 miriam-gene:3077, lld:C0018995; a sio:SIO_001122 . } dgn-np:NP782233.RANxac75KC5wmnyHpegDkncMsctW9QhRpO2EDMy5V3iIo130_provenance { dgn-np:NP782233.RANxac75KC5wmnyHpegDkncMsctW9QhRpO2EDMy5V3iIo130_assertion dcterms:description "[The MDM2 -309T > G promoter polymorphism, determining increased MDM2 and lower p53 activity, was associated with higher risk of hepatocarcinoma in cirrhotic patients with hemochromatosis, and with HFE mutations in patients with hepatocarcinoma without hemochromatosis, suggesting an interaction between MDM2 and iron in the pathogenesis of hepatocarcinoma.]. 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:20019189; 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:NP782233.RANxac75KC5wmnyHpegDkncMsctW9QhRpO2EDMy5V3iIo130_publicationInfo { this: dcterms:created "2016-05-13T12:47:39+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" . }