@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP704363.RAdqgQMPu7iF-TZlaTet2NB0YOAB2RwfE24QhNrxcb9CA> .
@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:NP704363.RAdqgQMPu7iF-TZlaTet2NB0YOAB2RwfE24QhNrxcb9CA130_head {
  this: np:hasAssertion dgn-np:NP704363.RAdqgQMPu7iF-TZlaTet2NB0YOAB2RwfE24QhNrxcb9CA130_assertion ;
    np:hasProvenance dgn-np:NP704363.RAdqgQMPu7iF-TZlaTet2NB0YOAB2RwfE24QhNrxcb9CA130_provenance ;
    np:hasPublicationInfo dgn-np:NP704363.RAdqgQMPu7iF-TZlaTet2NB0YOAB2RwfE24QhNrxcb9CA130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP704363.RAdqgQMPu7iF-TZlaTet2NB0YOAB2RwfE24QhNrxcb9CA130_assertion a np:Assertion .
  dgn-np:NP704363.RAdqgQMPu7iF-TZlaTet2NB0YOAB2RwfE24QhNrxcb9CA130_provenance a np:Provenance .
  dgn-np:NP704363.RAdqgQMPu7iF-TZlaTet2NB0YOAB2RwfE24QhNrxcb9CA130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP704363.RAdqgQMPu7iF-TZlaTet2NB0YOAB2RwfE24QhNrxcb9CA130_assertion {
  miriam-gene:64754 a ncit:C16612 .
  lld:C0596263 a ncit:C7057 .
  dgn-gda:DGN8c5bd69ff399c67872af2b6fa760ecba sio:SIO_000628 miriam-gene:64754 , lld:C0596263 ;
    a sio:SIO_001121 .
}
dgn-np:NP704363.RAdqgQMPu7iF-TZlaTet2NB0YOAB2RwfE24QhNrxcb9CA130_provenance {
  dgn-np:NP704363.RAdqgQMPu7iF-TZlaTet2NB0YOAB2RwfE24QhNrxcb9CA130_assertion dcterms:description "[A variable number of tandem repeats (VNTR) polymorphism in the promoter region of SMYD3, a recently characterized histone lysine methyltransferase gene that is implicated in cell proliferation and carcinogenesis, has been shown to be functional, but its association with cancer risk has not been well established because of apparently discrepant results in different populations.]. 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:18294291 ;
    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:NP704363.RAdqgQMPu7iF-TZlaTet2NB0YOAB2RwfE24QhNrxcb9CA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:08+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" .
}