@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:NP176789.RAt_6t0jZ8xtj7qHaL0dHK-09SfIistXk_bprBe8iRGD4130_head { this: np:hasAssertion dgn-np:NP176789.RAt_6t0jZ8xtj7qHaL0dHK-09SfIistXk_bprBe8iRGD4130_assertion; np:hasProvenance dgn-np:NP176789.RAt_6t0jZ8xtj7qHaL0dHK-09SfIistXk_bprBe8iRGD4130_provenance; np:hasPublicationInfo dgn-np:NP176789.RAt_6t0jZ8xtj7qHaL0dHK-09SfIistXk_bprBe8iRGD4130_publicationInfo; a np:Nanopublication . dgn-np:NP176789.RAt_6t0jZ8xtj7qHaL0dHK-09SfIistXk_bprBe8iRGD4130_assertion a np:Assertion . dgn-np:NP176789.RAt_6t0jZ8xtj7qHaL0dHK-09SfIistXk_bprBe8iRGD4130_provenance a np:Provenance . dgn-np:NP176789.RAt_6t0jZ8xtj7qHaL0dHK-09SfIistXk_bprBe8iRGD4130_publicationInfo a np:PublicationInfo . } dgn-np:NP176789.RAt_6t0jZ8xtj7qHaL0dHK-09SfIistXk_bprBe8iRGD4130_assertion { miriam-gene:7157 a ncit:C16612 . lld:C0023434 a ncit:C7057 . dgn-gda:DGN3375546472fff651617160e824c9ad61 sio:SIO_000628 miriam-gene:7157, lld:C0023434; a sio:SIO_001122 . } dgn-np:NP176789.RAt_6t0jZ8xtj7qHaL0dHK-09SfIistXk_bprBe8iRGD4130_provenance { dgn-np:NP176789.RAt_6t0jZ8xtj7qHaL0dHK-09SfIistXk_bprBe8iRGD4130_assertion dcterms:description "[In this report, with a high proportion of B-CLL patients with an advanced Binet stage and with an unmutated IgVH gene, MDM2 SNP309 was found to be independently associated with OS. The survival difference was more pronounced in younger patients.]. 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:20491880; prov:wasDerivedFrom dgn-void:gad-20150221; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP176789.RAt_6t0jZ8xtj7qHaL0dHK-09SfIistXk_bprBe8iRGD4130_publicationInfo { this: dcterms:created "2016-05-13T12:43:07+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" . }