@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP808705.RAbQ3CnejHQUoEmowckGuhMt1YszOSDy2vV6bj2PF6Nww> .
@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:NP808705.RAbQ3CnejHQUoEmowckGuhMt1YszOSDy2vV6bj2PF6Nww130_head {
  this: np:hasAssertion dgn-np:NP808705.RAbQ3CnejHQUoEmowckGuhMt1YszOSDy2vV6bj2PF6Nww130_assertion;
    np:hasProvenance dgn-np:NP808705.RAbQ3CnejHQUoEmowckGuhMt1YszOSDy2vV6bj2PF6Nww130_provenance;
    np:hasPublicationInfo dgn-np:NP808705.RAbQ3CnejHQUoEmowckGuhMt1YszOSDy2vV6bj2PF6Nww130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP808705.RAbQ3CnejHQUoEmowckGuhMt1YszOSDy2vV6bj2PF6Nww130_assertion a np:Assertion .
  
  dgn-np:NP808705.RAbQ3CnejHQUoEmowckGuhMt1YszOSDy2vV6bj2PF6Nww130_provenance a np:Provenance .
  
  dgn-np:NP808705.RAbQ3CnejHQUoEmowckGuhMt1YszOSDy2vV6bj2PF6Nww130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP808705.RAbQ3CnejHQUoEmowckGuhMt1YszOSDy2vV6bj2PF6Nww130_assertion {
  miriam-gene:1543 a ncit:C16612 .
  
  lld:C0346153 a ncit:C7057 .
  
  dgn-gda:DGNebdc64dcf808ee1b49beeb43efcd75e5 sio:SIO_000628 miriam-gene:1543, lld:C0346153;
    a sio:SIO_001121 .
}

dgn-np:NP808705.RAbQ3CnejHQUoEmowckGuhMt1YszOSDy2vV6bj2PF6Nww130_provenance {
  dgn-np:NP808705.RAbQ3CnejHQUoEmowckGuhMt1YszOSDy2vV6bj2PF6Nww130_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:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP808705.RAbQ3CnejHQUoEmowckGuhMt1YszOSDy2vV6bj2PF6Nww130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:16+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" .
}