@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP50969.RAKscAGyz3sWALQM1miomIK312e0pdsmvGe8rf0y6vhYg> .
@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:NP50969.RAKscAGyz3sWALQM1miomIK312e0pdsmvGe8rf0y6vhYg130_head {
  this: np:hasAssertion dgn-np:NP50969.RAKscAGyz3sWALQM1miomIK312e0pdsmvGe8rf0y6vhYg130_assertion;
    np:hasProvenance dgn-np:NP50969.RAKscAGyz3sWALQM1miomIK312e0pdsmvGe8rf0y6vhYg130_provenance;
    np:hasPublicationInfo dgn-np:NP50969.RAKscAGyz3sWALQM1miomIK312e0pdsmvGe8rf0y6vhYg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP50969.RAKscAGyz3sWALQM1miomIK312e0pdsmvGe8rf0y6vhYg130_assertion a np:Assertion .
  
  dgn-np:NP50969.RAKscAGyz3sWALQM1miomIK312e0pdsmvGe8rf0y6vhYg130_provenance a np:Provenance .
  
  dgn-np:NP50969.RAKscAGyz3sWALQM1miomIK312e0pdsmvGe8rf0y6vhYg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP50969.RAKscAGyz3sWALQM1miomIK312e0pdsmvGe8rf0y6vhYg130_assertion {
  miriam-gene:6817 a ncit:C16612 .
  
  lld:C0006142 a ncit:C7057 .
  
  dgn-gda:DGNf129349e1bb1af776c33d574344714be sio:SIO_000628 miriam-gene:6817, lld:C0006142;
    a sio:SIO_001122 .
}

dgn-np:NP50969.RAKscAGyz3sWALQM1miomIK312e0pdsmvGe8rf0y6vhYg130_provenance {
  dgn-np:NP50969.RAKscAGyz3sWALQM1miomIK312e0pdsmvGe8rf0y6vhYg130_assertion dcterms:description
      "[This case control study investigated whether polymorphisms of estrogen metabolizing genes CYP1A1 MspI, CYP17 MspAI, COMT Val(158) Met, and SULT1A1 Arg(213) His have any role in familial breast cancer susceptibility 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:19863350;
    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:NP50969.RAKscAGyz3sWALQM1miomIK312e0pdsmvGe8rf0y6vhYg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:23+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" .
}