@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP549450.RACDn9v9dcQOImstTN3GAwFDBMRdT36EZCSpV34WE-_D0> .
@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:NP549450.RACDn9v9dcQOImstTN3GAwFDBMRdT36EZCSpV34WE-_D0130_head {
  this: np:hasAssertion dgn-np:NP549450.RACDn9v9dcQOImstTN3GAwFDBMRdT36EZCSpV34WE-_D0130_assertion;
    np:hasProvenance dgn-np:NP549450.RACDn9v9dcQOImstTN3GAwFDBMRdT36EZCSpV34WE-_D0130_provenance;
    np:hasPublicationInfo dgn-np:NP549450.RACDn9v9dcQOImstTN3GAwFDBMRdT36EZCSpV34WE-_D0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP549450.RACDn9v9dcQOImstTN3GAwFDBMRdT36EZCSpV34WE-_D0130_assertion a np:Assertion .
  
  dgn-np:NP549450.RACDn9v9dcQOImstTN3GAwFDBMRdT36EZCSpV34WE-_D0130_provenance a np:Provenance .
  
  dgn-np:NP549450.RACDn9v9dcQOImstTN3GAwFDBMRdT36EZCSpV34WE-_D0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP549450.RACDn9v9dcQOImstTN3GAwFDBMRdT36EZCSpV34WE-_D0130_assertion {
  miriam-gene:10200 a ncit:C16612 .
  
  lld:C0007097 a ncit:C7057 .
  
  dgn-gda:DGN0252faf4a3a9ae370948a64ddf0d3dd1 sio:SIO_000628 miriam-gene:10200, lld:C0007097;
    a sio:SIO_001121 .
}

dgn-np:NP549450.RACDn9v9dcQOImstTN3GAwFDBMRdT36EZCSpV34WE-_D0130_provenance {
  dgn-np:NP549450.RACDn9v9dcQOImstTN3GAwFDBMRdT36EZCSpV34WE-_D0130_assertion dcterms:description
      "[We found that the frequencies of GSTP1 genotypes based on the Ile105 and Val105-expressing alleles and CCND1 AA, AG, GG genotypes were similar in MPP and SPP cases and that there were no significant associations between GSTP1 or CCND1 genotypes and BCC numbers in the total or SPP groups.]. 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:10975609;
    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:NP549450.RACDn9v9dcQOImstTN3GAwFDBMRdT36EZCSpV34WE-_D0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:31+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" .
}