@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP59908.RAuMNIXo4rdbC7VNiw6uWsilZxc-XpeWfQLMTvKPfHQus> .
@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:NP59908.RAuMNIXo4rdbC7VNiw6uWsilZxc-XpeWfQLMTvKPfHQus130_head {
  this: np:hasAssertion dgn-np:NP59908.RAuMNIXo4rdbC7VNiw6uWsilZxc-XpeWfQLMTvKPfHQus130_assertion;
    np:hasProvenance dgn-np:NP59908.RAuMNIXo4rdbC7VNiw6uWsilZxc-XpeWfQLMTvKPfHQus130_provenance;
    np:hasPublicationInfo dgn-np:NP59908.RAuMNIXo4rdbC7VNiw6uWsilZxc-XpeWfQLMTvKPfHQus130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP59908.RAuMNIXo4rdbC7VNiw6uWsilZxc-XpeWfQLMTvKPfHQus130_assertion a np:Assertion .
  
  dgn-np:NP59908.RAuMNIXo4rdbC7VNiw6uWsilZxc-XpeWfQLMTvKPfHQus130_provenance a np:Provenance .
  
  dgn-np:NP59908.RAuMNIXo4rdbC7VNiw6uWsilZxc-XpeWfQLMTvKPfHQus130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP59908.RAuMNIXo4rdbC7VNiw6uWsilZxc-XpeWfQLMTvKPfHQus130_assertion {
  miriam-gene:1312 a ncit:C16612 .
  
  lld:C0006142 a ncit:C7057 .
  
  dgn-gda:DGNf89c187980bdab8491d559587c1b9315 sio:SIO_000628 miriam-gene:1312, lld:C0006142;
    a sio:SIO_001122 .
}

dgn-np:NP59908.RAuMNIXo4rdbC7VNiw6uWsilZxc-XpeWfQLMTvKPfHQus130_provenance {
  dgn-np:NP59908.RAuMNIXo4rdbC7VNiw6uWsilZxc-XpeWfQLMTvKPfHQus130_assertion dcterms:description
      "[These studies showed that two SNPs in the COMT distal promoter were associated with breast cancer risk reduction in two of three case control studies, compatible with the results of functional genomic experiments, suggesting a role for MB-COMT in breast cancer risk.]. 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:18632656;
    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:NP59908.RAuMNIXo4rdbC7VNiw6uWsilZxc-XpeWfQLMTvKPfHQus130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:28+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" .
}