@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP46210.RA1XQ0O2lH4wzUR6SlaU_klQgC277ah1fAoQsCA4LARiQ> .
@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:NP46210.RA1XQ0O2lH4wzUR6SlaU_klQgC277ah1fAoQsCA4LARiQ130_head {
  this: np:hasAssertion dgn-np:NP46210.RA1XQ0O2lH4wzUR6SlaU_klQgC277ah1fAoQsCA4LARiQ130_assertion;
    np:hasProvenance dgn-np:NP46210.RA1XQ0O2lH4wzUR6SlaU_klQgC277ah1fAoQsCA4LARiQ130_provenance;
    np:hasPublicationInfo dgn-np:NP46210.RA1XQ0O2lH4wzUR6SlaU_klQgC277ah1fAoQsCA4LARiQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP46210.RA1XQ0O2lH4wzUR6SlaU_klQgC277ah1fAoQsCA4LARiQ130_assertion a np:Assertion .
  
  dgn-np:NP46210.RA1XQ0O2lH4wzUR6SlaU_klQgC277ah1fAoQsCA4LARiQ130_provenance a np:Provenance .
  
  dgn-np:NP46210.RA1XQ0O2lH4wzUR6SlaU_klQgC277ah1fAoQsCA4LARiQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP46210.RA1XQ0O2lH4wzUR6SlaU_klQgC277ah1fAoQsCA4LARiQ130_assertion {
  miriam-gene:1586 a ncit:C16612 .
  
  lld:C1846502 a ncit:C7057 .
  
  dgn-gda:DGN2c03ae997da3d4466ccdafe2877fa6b2 sio:SIO_000628 miriam-gene:1586, lld:C1846502;
    a sio:SIO_001122 .
}

dgn-np:NP46210.RA1XQ0O2lH4wzUR6SlaU_klQgC277ah1fAoQsCA4LARiQ130_provenance {
  dgn-np:NP46210.RA1XQ0O2lH4wzUR6SlaU_klQgC277ah1fAoQsCA4LARiQ130_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: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:NP46210.RA1XQ0O2lH4wzUR6SlaU_klQgC277ah1fAoQsCA4LARiQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:21+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" .
}