@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:NP411691.RA8zkSw1hQg4hcbuN3482ut3slEHBfI4soMSXgB4BnKeA130_head { this: np:hasAssertion dgn-np:NP411691.RA8zkSw1hQg4hcbuN3482ut3slEHBfI4soMSXgB4BnKeA130_assertion; np:hasProvenance dgn-np:NP411691.RA8zkSw1hQg4hcbuN3482ut3slEHBfI4soMSXgB4BnKeA130_provenance; np:hasPublicationInfo dgn-np:NP411691.RA8zkSw1hQg4hcbuN3482ut3slEHBfI4soMSXgB4BnKeA130_publicationInfo; a np:Nanopublication . dgn-np:NP411691.RA8zkSw1hQg4hcbuN3482ut3slEHBfI4soMSXgB4BnKeA130_assertion a np:Assertion . dgn-np:NP411691.RA8zkSw1hQg4hcbuN3482ut3slEHBfI4soMSXgB4BnKeA130_provenance a np:Provenance . dgn-np:NP411691.RA8zkSw1hQg4hcbuN3482ut3slEHBfI4soMSXgB4BnKeA130_publicationInfo a np:PublicationInfo . } dgn-np:NP411691.RA8zkSw1hQg4hcbuN3482ut3slEHBfI4soMSXgB4BnKeA130_assertion { miriam-gene:2463 a ncit:C16612 . lld:C1882062 a ncit:C7057 . dgn-gda:DGNe1f17a04b06295bff97911d47ae71e3a sio:SIO_000628 miriam-gene:2463, lld:C1882062; a sio:SIO_001121 . } dgn-np:NP411691.RA8zkSw1hQg4hcbuN3482ut3slEHBfI4soMSXgB4BnKeA130_provenance { dgn-np:NP411691.RA8zkSw1hQg4hcbuN3482ut3slEHBfI4soMSXgB4BnKeA130_assertion dcterms:description "[The major aim of the present study was to determine whether the FRA16D chromosomal fragile site locus has a role to play in predisposing DNA sequences within and adjacent to the fragile site to DNA instability (such as deletion or translocation), which could lead to or be associated with neoplasia.]. 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:10749140; 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:NP411691.RA8zkSw1hQg4hcbuN3482ut3slEHBfI4soMSXgB4BnKeA130_publicationInfo { this: dcterms:created "2015-08-25T14:41:39+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 "v3.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v3.0.0" . }