@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP743728.RAgyLTsyI1EAnWx2l5R25onLyhUV6ffsok77QnuFpsFYI> .
@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:NP743728.RAgyLTsyI1EAnWx2l5R25onLyhUV6ffsok77QnuFpsFYI130_head {
   this: np:hasAssertion dgn-np:NP743728.RAgyLTsyI1EAnWx2l5R25onLyhUV6ffsok77QnuFpsFYI130_assertion ;
    np:hasProvenance dgn-np:NP743728.RAgyLTsyI1EAnWx2l5R25onLyhUV6ffsok77QnuFpsFYI130_provenance ;
    np:hasPublicationInfo dgn-np:NP743728.RAgyLTsyI1EAnWx2l5R25onLyhUV6ffsok77QnuFpsFYI130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP743728.RAgyLTsyI1EAnWx2l5R25onLyhUV6ffsok77QnuFpsFYI130_assertion a np:Assertion .
  dgn-np:NP743728.RAgyLTsyI1EAnWx2l5R25onLyhUV6ffsok77QnuFpsFYI130_provenance a np:Provenance .
  dgn-np:NP743728.RAgyLTsyI1EAnWx2l5R25onLyhUV6ffsok77QnuFpsFYI130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP743728.RAgyLTsyI1EAnWx2l5R25onLyhUV6ffsok77QnuFpsFYI130_assertion {
   miriam-gene:26523 a ncit:C16612 .
  lld:C0007134 a ncit:C7057 .
  dgn-gda:DGNb4157047b3bd4616bce4a99ae16c28d9 sio:SIO_000628 miriam-gene:26523 , lld:C0007134 ;
    a sio:SIO_001121 .
}
dgn-np:NP743728.RAgyLTsyI1EAnWx2l5R25onLyhUV6ffsok77QnuFpsFYI130_provenance {
   dgn-np:NP743728.RAgyLTsyI1EAnWx2l5R25onLyhUV6ffsok77QnuFpsFYI130_assertion dcterms:description "[We genotyped 40 single nucleotide polymorphisms (SNP) from 11 miRNA processing genes (DROSHA, DGCR8, XPO5, RAN, DICER1, TARBP2, AGO1, AGO2, GEMIN3, GEMIN4, HIWI) and 15 miRNA genes in 279 Caucasian patients with renal cell carcinoma and 278 matched controls.]. 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:19047128 ;
    prov:wasDerivedFrom dgn-void:befree-20140225 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP743728.RAgyLTsyI1EAnWx2l5R25onLyhUV6ffsok77QnuFpsFYI130_publicationInfo {
   this: dcterms:created "2014-10-02T12:39:31+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" .
}