@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP84788.RAAmXIqgWuNIJv1TFyurOoagNBGeSqMbtjQQ6ykj37fuk> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix eco: <http://purl.obolibrary.org/obo/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .
dgn-np:NP84788.RAAmXIqgWuNIJv1TFyurOoagNBGeSqMbtjQQ6ykj37fuk130_head {
  this: np:hasAssertion dgn-np:NP84788.RAAmXIqgWuNIJv1TFyurOoagNBGeSqMbtjQQ6ykj37fuk130_assertion ;
    np:hasProvenance dgn-np:NP84788.RAAmXIqgWuNIJv1TFyurOoagNBGeSqMbtjQQ6ykj37fuk130_provenance ;
    np:hasPublicationInfo dgn-np:NP84788.RAAmXIqgWuNIJv1TFyurOoagNBGeSqMbtjQQ6ykj37fuk130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP84788.RAAmXIqgWuNIJv1TFyurOoagNBGeSqMbtjQQ6ykj37fuk130_assertion a np:Assertion .
  dgn-np:NP84788.RAAmXIqgWuNIJv1TFyurOoagNBGeSqMbtjQQ6ykj37fuk130_provenance a np:Provenance .
  dgn-np:NP84788.RAAmXIqgWuNIJv1TFyurOoagNBGeSqMbtjQQ6ykj37fuk130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP84788.RAAmXIqgWuNIJv1TFyurOoagNBGeSqMbtjQQ6ykj37fuk130_assertion {
  miriam-gene:406983 a ncit:C16612 .
  lld:C1140680 a ncit:C7057 .
  dgn-gda:DGNbc777f29653ef14a6fe57abd754c78d8 sio:SIO_000628 miriam-gene:406983 , lld:C1140680 ;
    a sio:SIO_001122 .
}
dgn-np:NP84788.RAAmXIqgWuNIJv1TFyurOoagNBGeSqMbtjQQ6ykj37fuk130_provenance {
  dgn-np:NP84788.RAAmXIqgWuNIJv1TFyurOoagNBGeSqMbtjQQ6ykj37fuk130_assertion dcterms:description "[Our findings suggest that there are novel genetic variants in miRNA genes, and those certain genetic variants in miRNA genes can affect the expression of mature miRNAs and, consequently, might alter the regulation of TSGs or oncogenes. Additionally, the variant might be potentially associated with the development of familial ovarian cancer.]. 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:20167074 ;
    prov:wasDerivedFrom dgn-void:gad-20130706 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP84788.RAAmXIqgWuNIJv1TFyurOoagNBGeSqMbtjQQ6ykj37fuk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:42+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
    prv:usedData dgn-void:disgenetrdf ;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269> , <http://orcid.org/0000-0002-7534-7661> , <http://orcid.org/0000-0002-9383-528X> , <http://orcid.org/0000-0003-0169-8159> , <http://orcid.org/0000-0003-1244-7654> ;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159> ;
    pav:version "v2.1.0.0" .
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}