@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:NP1134034.RAwhiftnmlgkXGYoPFFVf69I38xTijOMOrwLBqQiWh9B8130_head { this: np:hasAssertion dgn-np:NP1134034.RAwhiftnmlgkXGYoPFFVf69I38xTijOMOrwLBqQiWh9B8130_assertion; np:hasProvenance dgn-np:NP1134034.RAwhiftnmlgkXGYoPFFVf69I38xTijOMOrwLBqQiWh9B8130_provenance; np:hasPublicationInfo dgn-np:NP1134034.RAwhiftnmlgkXGYoPFFVf69I38xTijOMOrwLBqQiWh9B8130_publicationInfo; a np:Nanopublication . dgn-np:NP1134034.RAwhiftnmlgkXGYoPFFVf69I38xTijOMOrwLBqQiWh9B8130_assertion a np:Assertion . dgn-np:NP1134034.RAwhiftnmlgkXGYoPFFVf69I38xTijOMOrwLBqQiWh9B8130_provenance a np:Provenance . dgn-np:NP1134034.RAwhiftnmlgkXGYoPFFVf69I38xTijOMOrwLBqQiWh9B8130_publicationInfo a np:PublicationInfo . } dgn-np:NP1134034.RAwhiftnmlgkXGYoPFFVf69I38xTijOMOrwLBqQiWh9B8130_assertion { miriam-gene:639 a ncit:C16612 . lld:C0027627 a ncit:C7057 . dgn-gda:DGNa2b94523aeb5d652ea4bfbffa413ec81 sio:SIO_000628 miriam-gene:639, lld:C0027627; a sio:SIO_001122 . } dgn-np:NP1134034.RAwhiftnmlgkXGYoPFFVf69I38xTijOMOrwLBqQiWh9B8130_provenance { dgn-np:NP1134034.RAwhiftnmlgkXGYoPFFVf69I38xTijOMOrwLBqQiWh9B8130_assertion dcterms:description "[Recent GWAS study identified rs4946728 and rs1040411 noncoding SNPs located between PRDM1 and ATG1 genes on chromosome 6q21 as risk factors for secondary malignancies in patients formerly treated with radiotherapy for pediatric Hodgkin disease.]. 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:24306881; 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:NP1134034.RAwhiftnmlgkXGYoPFFVf69I38xTijOMOrwLBqQiWh9B8130_publicationInfo { this: dcterms:created "2016-05-13T12:50:20+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" . }