@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP846830.RAzj7IN9lsHD5LquFnt7V-MhH4brsZ4eozPtv_qfuLqAw> .
@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:NP846830.RAzj7IN9lsHD5LquFnt7V-MhH4brsZ4eozPtv_qfuLqAw130_head {
  this: np:hasAssertion dgn-np:NP846830.RAzj7IN9lsHD5LquFnt7V-MhH4brsZ4eozPtv_qfuLqAw130_assertion;
    np:hasProvenance dgn-np:NP846830.RAzj7IN9lsHD5LquFnt7V-MhH4brsZ4eozPtv_qfuLqAw130_provenance;
    np:hasPublicationInfo dgn-np:NP846830.RAzj7IN9lsHD5LquFnt7V-MhH4brsZ4eozPtv_qfuLqAw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP846830.RAzj7IN9lsHD5LquFnt7V-MhH4brsZ4eozPtv_qfuLqAw130_assertion a np:Assertion .
  
  dgn-np:NP846830.RAzj7IN9lsHD5LquFnt7V-MhH4brsZ4eozPtv_qfuLqAw130_provenance a np:Provenance .
  
  dgn-np:NP846830.RAzj7IN9lsHD5LquFnt7V-MhH4brsZ4eozPtv_qfuLqAw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP846830.RAzj7IN9lsHD5LquFnt7V-MhH4brsZ4eozPtv_qfuLqAw130_assertion {
  miriam-gene:3553 a ncit:C16612 .
  
  lld:C2827470 a ncit:C7057 .
  
  dgn-gda:DGN4950443553b7c16c8c3992c3cf87f25e sio:SIO_000628 miriam-gene:3553, lld:C2827470;
    a sio:SIO_001121 .
}

dgn-np:NP846830.RAzj7IN9lsHD5LquFnt7V-MhH4brsZ4eozPtv_qfuLqAw130_provenance {
  dgn-np:NP846830.RAzj7IN9lsHD5LquFnt7V-MhH4brsZ4eozPtv_qfuLqAw130_assertion dcterms:description
      "[In a case-control study on the causes of deep venous thrombosis, the Leiden Thrombophilia Study (LETS), we genotyped 18 single nucleotide polymorphisms (SNPs) in IL1B, IL1RN, IL1R1, and IL1R2, enabling us to tag a total of 25 haplotype 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:17413037;
    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:NP846830.RAzj7IN9lsHD5LquFnt7V-MhH4brsZ4eozPtv_qfuLqAw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:37+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" .
}