@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP322232.RA8SAEQEJk4nUM0Q_yewq_U5qXtE0Hbwj72wcpOQsU5C8> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP322232.RA8SAEQEJk4nUM0Q_yewq_U5qXtE0Hbwj72wcpOQsU5C8130_head {
  this: np:hasAssertion dgn-np:NP322232.RA8SAEQEJk4nUM0Q_yewq_U5qXtE0Hbwj72wcpOQsU5C8130_assertion;
    np:hasProvenance dgn-np:NP322232.RA8SAEQEJk4nUM0Q_yewq_U5qXtE0Hbwj72wcpOQsU5C8130_provenance;
    np:hasPublicationInfo dgn-np:NP322232.RA8SAEQEJk4nUM0Q_yewq_U5qXtE0Hbwj72wcpOQsU5C8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP322232.RA8SAEQEJk4nUM0Q_yewq_U5qXtE0Hbwj72wcpOQsU5C8130_assertion a np:Assertion .
  
  dgn-np:NP322232.RA8SAEQEJk4nUM0Q_yewq_U5qXtE0Hbwj72wcpOQsU5C8130_provenance a np:Provenance .
  
  dgn-np:NP322232.RA8SAEQEJk4nUM0Q_yewq_U5qXtE0Hbwj72wcpOQsU5C8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP322232.RA8SAEQEJk4nUM0Q_yewq_U5qXtE0Hbwj72wcpOQsU5C8130_assertion {
  miriam-gene:1312 a ncit:C16612 .
  
  lld:C1846502 a ncit:C7057 .
  
  dgn-gda:DGNf96cd824b9a743dad889376ec26a45ec sio:SIO_000628 miriam-gene:1312, lld:C1846502;
    a sio:SIO_001121 .
}

dgn-np:NP322232.RA8SAEQEJk4nUM0Q_yewq_U5qXtE0Hbwj72wcpOQsU5C8130_provenance {
  dgn-np:NP322232.RA8SAEQEJk4nUM0Q_yewq_U5qXtE0Hbwj72wcpOQsU5C8130_assertion dcterms:description
      "[Our data suggest lower mammographic density for women carrying the COMT and CYP1A2 variant alleles than for women carrying the common alleles, though this is the opposite of what is commonly hypothesized from the enzyme function.]. 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:15382051;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP322232.RA8SAEQEJk4nUM0Q_yewq_U5qXtE0Hbwj72wcpOQsU5C8130_publicationInfo {
  this: dcterms:created "2015-08-25T14:40:45+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}