@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP67304.RAUylPtCI0245MeYG4M9JBgX2FvrTccpteZv3l53HrbZ4> .
@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:NP67304.RAUylPtCI0245MeYG4M9JBgX2FvrTccpteZv3l53HrbZ4130_head {
  this: np:hasAssertion dgn-np:NP67304.RAUylPtCI0245MeYG4M9JBgX2FvrTccpteZv3l53HrbZ4130_assertion;
    np:hasProvenance dgn-np:NP67304.RAUylPtCI0245MeYG4M9JBgX2FvrTccpteZv3l53HrbZ4130_provenance;
    np:hasPublicationInfo dgn-np:NP67304.RAUylPtCI0245MeYG4M9JBgX2FvrTccpteZv3l53HrbZ4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP67304.RAUylPtCI0245MeYG4M9JBgX2FvrTccpteZv3l53HrbZ4130_assertion a np:Assertion .
  
  dgn-np:NP67304.RAUylPtCI0245MeYG4M9JBgX2FvrTccpteZv3l53HrbZ4130_provenance a np:Provenance .
  
  dgn-np:NP67304.RAUylPtCI0245MeYG4M9JBgX2FvrTccpteZv3l53HrbZ4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP67304.RAUylPtCI0245MeYG4M9JBgX2FvrTccpteZv3l53HrbZ4130_assertion {
  miriam-gene:1583 a ncit:C16612 .
  
  lld:C0032460 a ncit:C7057 .
  
  dgn-gda:DGN9cb37c6f0cd06cccd73ab018c5eda9e8 sio:SIO_000628 miriam-gene:1583, lld:C0032460;
    a sio:SIO_001122 .
}

dgn-np:NP67304.RAUylPtCI0245MeYG4M9JBgX2FvrTccpteZv3l53HrbZ4130_provenance {
  dgn-np:NP67304.RAUylPtCI0245MeYG4M9JBgX2FvrTccpteZv3l53HrbZ4130_assertion dcterms:description
      "[indicate that common alleles of the CYP11alpha promoter pentannucleotide (tttta)n polymorphism in this population of Han Chinese women were P4, P6 and P8, and allele P6 was the most common one.]. 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:19300392;
    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:NP67304.RAUylPtCI0245MeYG4M9JBgX2FvrTccpteZv3l53HrbZ4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:32+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" .
}