@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP264070.RAsskjyMymUPglEhP2WsGCmXlqsJ7vdds5kbdPz1br9SA> .
@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:NP264070.RAsskjyMymUPglEhP2WsGCmXlqsJ7vdds5kbdPz1br9SA130_head {
  this: np:hasAssertion dgn-np:NP264070.RAsskjyMymUPglEhP2WsGCmXlqsJ7vdds5kbdPz1br9SA130_assertion;
    np:hasProvenance dgn-np:NP264070.RAsskjyMymUPglEhP2WsGCmXlqsJ7vdds5kbdPz1br9SA130_provenance;
    np:hasPublicationInfo dgn-np:NP264070.RAsskjyMymUPglEhP2WsGCmXlqsJ7vdds5kbdPz1br9SA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP264070.RAsskjyMymUPglEhP2WsGCmXlqsJ7vdds5kbdPz1br9SA130_assertion a np:Assertion .
  
  dgn-np:NP264070.RAsskjyMymUPglEhP2WsGCmXlqsJ7vdds5kbdPz1br9SA130_provenance a np:Provenance .
  
  dgn-np:NP264070.RAsskjyMymUPglEhP2WsGCmXlqsJ7vdds5kbdPz1br9SA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP264070.RAsskjyMymUPglEhP2WsGCmXlqsJ7vdds5kbdPz1br9SA130_assertion {
  miriam-gene:2099 a ncit:C16612 .
  
  lld:C0009402 a ncit:C7057 .
  
  dgn-gda:DGNf9796a62a420c4172aa580069dadaf6a sio:SIO_000628 miriam-gene:2099, lld:C0009402;
    a sio:SIO_001121 .
}

dgn-np:NP264070.RAsskjyMymUPglEhP2WsGCmXlqsJ7vdds5kbdPz1br9SA130_provenance {
  dgn-np:NP264070.RAsskjyMymUPglEhP2WsGCmXlqsJ7vdds5kbdPz1br9SA130_assertion dcterms:description
      "[We conducted a comprehensive evaluation of single nucleotide polymorphisms (SNPs) in genes encoding 3 hormone receptors (ESR1, ESR2, PGR) and 5 hormone synthesizers (CYP19A1 and CYP17A1, HSD17B1, HSD17B2, HSD17B4) among 427 women with incident colorectal cancer and 871 matched controls who were Caucasians of European ancestry from 93676 postmenopausal women enrolled in the Women's Health Initiative Observational cohort.]. 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:21627810;
    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:NP264070.RAsskjyMymUPglEhP2WsGCmXlqsJ7vdds5kbdPz1br9SA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:27+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" .
}