@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP215778.RA3gyB0Apa55BBYxE8v1djiD1L9_YCfFJQihzwd8rlMl8> .
@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:NP215778.RA3gyB0Apa55BBYxE8v1djiD1L9_YCfFJQihzwd8rlMl8130_head {
  this: np:hasAssertion dgn-np:NP215778.RA3gyB0Apa55BBYxE8v1djiD1L9_YCfFJQihzwd8rlMl8130_assertion;
    np:hasProvenance dgn-np:NP215778.RA3gyB0Apa55BBYxE8v1djiD1L9_YCfFJQihzwd8rlMl8130_provenance;
    np:hasPublicationInfo dgn-np:NP215778.RA3gyB0Apa55BBYxE8v1djiD1L9_YCfFJQihzwd8rlMl8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP215778.RA3gyB0Apa55BBYxE8v1djiD1L9_YCfFJQihzwd8rlMl8130_assertion a np:Assertion .
  
  dgn-np:NP215778.RA3gyB0Apa55BBYxE8v1djiD1L9_YCfFJQihzwd8rlMl8130_provenance a np:Provenance .
  
  dgn-np:NP215778.RA3gyB0Apa55BBYxE8v1djiD1L9_YCfFJQihzwd8rlMl8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP215778.RA3gyB0Apa55BBYxE8v1djiD1L9_YCfFJQihzwd8rlMl8130_assertion {
  miriam-gene:1586 a ncit:C16612 .
  
  lld:C1527249 a ncit:C7057 .
  
  dgn-gda:DGNa044471a984d9a0f66e52af75ddb672f sio:SIO_000628 miriam-gene:1586, lld:C1527249;
    a sio:SIO_001121 .
}

dgn-np:NP215778.RA3gyB0Apa55BBYxE8v1djiD1L9_YCfFJQihzwd8rlMl8130_provenance {
  dgn-np:NP215778.RA3gyB0Apa55BBYxE8v1djiD1L9_YCfFJQihzwd8rlMl8130_assertion dcterms:description
      "[To investigate if common variants of CYP1A2, CYP1B1, CYP3A4, CYP3A5, CYP11A1, CYP17A1 and CYP19A1 influence CRC risk we genotyped 2,575 CRC cases and 2,707 controls for 20 single nucleotide polymorphisms (SNPs) that have not previously been shown to have functional consequence within these genes.]. 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:17615053;
    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:NP215778.RA3gyB0Apa55BBYxE8v1djiD1L9_YCfFJQihzwd8rlMl8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:59+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" .
}