@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP45882.RAr7Hzmn3-sojKvXFlw5yon2FtyPbWZCAiJVox0WTz5G0> .
@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 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:NP45882.RAr7Hzmn3-sojKvXFlw5yon2FtyPbWZCAiJVox0WTz5G0130_head {
  this: np:hasAssertion dgn-np:NP45882.RAr7Hzmn3-sojKvXFlw5yon2FtyPbWZCAiJVox0WTz5G0130_assertion;
    np:hasProvenance dgn-np:NP45882.RAr7Hzmn3-sojKvXFlw5yon2FtyPbWZCAiJVox0WTz5G0130_provenance;
    np:hasPublicationInfo dgn-np:NP45882.RAr7Hzmn3-sojKvXFlw5yon2FtyPbWZCAiJVox0WTz5G0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP45882.RAr7Hzmn3-sojKvXFlw5yon2FtyPbWZCAiJVox0WTz5G0130_assertion a np:Assertion .
  
  dgn-np:NP45882.RAr7Hzmn3-sojKvXFlw5yon2FtyPbWZCAiJVox0WTz5G0130_provenance a np:Provenance .
  
  dgn-np:NP45882.RAr7Hzmn3-sojKvXFlw5yon2FtyPbWZCAiJVox0WTz5G0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP45882.RAr7Hzmn3-sojKvXFlw5yon2FtyPbWZCAiJVox0WTz5G0130_assertion {
  miriam-gene:1545 a ncit:C16612 .
  
  lld:C1846502 a ncit:C7057 .
  
  dgn-gda:DGNe3ce983e7447b49b10cb6e9b37701a52 sio:SIO_000628 miriam-gene:1545, lld:C1846502;
    a sio:SIO_001122 .
}

dgn-np:NP45882.RAr7Hzmn3-sojKvXFlw5yon2FtyPbWZCAiJVox0WTz5G0130_provenance {
  dgn-np:NP45882.RAr7Hzmn3-sojKvXFlw5yon2FtyPbWZCAiJVox0WTz5G0130_assertion dct: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:NP45882.RAr7Hzmn3-sojKvXFlw5yon2FtyPbWZCAiJVox0WTz5G0130_publicationInfo {
  this: dct:created "2014-10-02T12:32:21+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}