@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP60052.RAX0hwt8WBSQHHPUc1U2HSTGVaAU7C09sTV-m-EpPfZC4> .
@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:NP60052.RAX0hwt8WBSQHHPUc1U2HSTGVaAU7C09sTV-m-EpPfZC4130_head {
  this: np:hasAssertion dgn-np:NP60052.RAX0hwt8WBSQHHPUc1U2HSTGVaAU7C09sTV-m-EpPfZC4130_assertion;
    np:hasProvenance dgn-np:NP60052.RAX0hwt8WBSQHHPUc1U2HSTGVaAU7C09sTV-m-EpPfZC4130_provenance;
    np:hasPublicationInfo dgn-np:NP60052.RAX0hwt8WBSQHHPUc1U2HSTGVaAU7C09sTV-m-EpPfZC4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP60052.RAX0hwt8WBSQHHPUc1U2HSTGVaAU7C09sTV-m-EpPfZC4130_assertion a np:Assertion .
  
  dgn-np:NP60052.RAX0hwt8WBSQHHPUc1U2HSTGVaAU7C09sTV-m-EpPfZC4130_provenance a np:Provenance .
  
  dgn-np:NP60052.RAX0hwt8WBSQHHPUc1U2HSTGVaAU7C09sTV-m-EpPfZC4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP60052.RAX0hwt8WBSQHHPUc1U2HSTGVaAU7C09sTV-m-EpPfZC4130_assertion {
  miriam-gene:1565 a ncit:C16612 .
  
  lld:C0151526 a ncit:C7057 .
  
  dgn-gda:DGN74409845d2107635ed7c2a1717bf4af9 sio:SIO_000628 miriam-gene:1565, lld:C0151526;
    a sio:SIO_001122 .
}

dgn-np:NP60052.RAX0hwt8WBSQHHPUc1U2HSTGVaAU7C09sTV-m-EpPfZC4130_provenance {
  dgn-np:NP60052.RAX0hwt8WBSQHHPUc1U2HSTGVaAU7C09sTV-m-EpPfZC4130_assertion dcterms:description
      "[This study integrates epidemiological and clinical data as well as genetic markers along major pathogenic pathways of PTD. The findings from this study should improve our understanding of genetic influences on PTD and gene-environment interactions.]. 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:11520401;
    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:NP60052.RAX0hwt8WBSQHHPUc1U2HSTGVaAU7C09sTV-m-EpPfZC4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:28+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" .
}