@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP247104.RAhMrqoZ-LlsVJt0yECY3rZk_ONLjxDmwtgxWzDmfuYQQ> .
@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:NP247104.RAhMrqoZ-LlsVJt0yECY3rZk_ONLjxDmwtgxWzDmfuYQQ130_head {
  this: np:hasAssertion dgn-np:NP247104.RAhMrqoZ-LlsVJt0yECY3rZk_ONLjxDmwtgxWzDmfuYQQ130_assertion;
    np:hasProvenance dgn-np:NP247104.RAhMrqoZ-LlsVJt0yECY3rZk_ONLjxDmwtgxWzDmfuYQQ130_provenance;
    np:hasPublicationInfo dgn-np:NP247104.RAhMrqoZ-LlsVJt0yECY3rZk_ONLjxDmwtgxWzDmfuYQQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP247104.RAhMrqoZ-LlsVJt0yECY3rZk_ONLjxDmwtgxWzDmfuYQQ130_assertion a np:Assertion .
  
  dgn-np:NP247104.RAhMrqoZ-LlsVJt0yECY3rZk_ONLjxDmwtgxWzDmfuYQQ130_provenance a np:Provenance .
  
  dgn-np:NP247104.RAhMrqoZ-LlsVJt0yECY3rZk_ONLjxDmwtgxWzDmfuYQQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP247104.RAhMrqoZ-LlsVJt0yECY3rZk_ONLjxDmwtgxWzDmfuYQQ130_assertion {
  miriam-gene:64754 a ncit:C16612 .
  
  lld:C1527249 a ncit:C7057 .
  
  dgn-gda:DGN60d604e0be6f63d7420f1a36109319e0 sio:SIO_000628 miriam-gene:64754, lld:C1527249;
    a sio:SIO_001121 .
}

dgn-np:NP247104.RAhMrqoZ-LlsVJt0yECY3rZk_ONLjxDmwtgxWzDmfuYQQ130_provenance {
  dgn-np:NP247104.RAhMrqoZ-LlsVJt0yECY3rZk_ONLjxDmwtgxWzDmfuYQQ130_assertion dcterms:description
      "[A variable number of tandem repeats (VNTR) polymorphism in regulatory region of SMYD3 coding for histone methyltransferase has been shown to be associated with colorectal cancer, hepatocellular carcinoma (HCC), and breast cancer in Japanese population.]. 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:17431393;
    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:NP247104.RAhMrqoZ-LlsVJt0yECY3rZk_ONLjxDmwtgxWzDmfuYQQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:18+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" .
}