@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP75158.RA3MsYC0GKrSv_vd94i_jqOc95iXvtUm26B96rBfFYhy0> .
@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:NP75158.RA3MsYC0GKrSv_vd94i_jqOc95iXvtUm26B96rBfFYhy0130_head {
  this: np:hasAssertion dgn-np:NP75158.RA3MsYC0GKrSv_vd94i_jqOc95iXvtUm26B96rBfFYhy0130_assertion;
    np:hasProvenance dgn-np:NP75158.RA3MsYC0GKrSv_vd94i_jqOc95iXvtUm26B96rBfFYhy0130_provenance;
    np:hasPublicationInfo dgn-np:NP75158.RA3MsYC0GKrSv_vd94i_jqOc95iXvtUm26B96rBfFYhy0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP75158.RA3MsYC0GKrSv_vd94i_jqOc95iXvtUm26B96rBfFYhy0130_assertion a np:Assertion .
  
  dgn-np:NP75158.RA3MsYC0GKrSv_vd94i_jqOc95iXvtUm26B96rBfFYhy0130_provenance a np:Provenance .
  
  dgn-np:NP75158.RA3MsYC0GKrSv_vd94i_jqOc95iXvtUm26B96rBfFYhy0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP75158.RA3MsYC0GKrSv_vd94i_jqOc95iXvtUm26B96rBfFYhy0130_assertion {
  miriam-gene:2147 a ncit:C16612 .
  
  lld:C0398623 a ncit:C7057 .
  
  dgn-gda:DGN2824735be3fc26ccb98510fd7e4c4290 sio:SIO_000628 miriam-gene:2147, lld:C0398623;
    a sio:SIO_001122 .
}

dgn-np:NP75158.RA3MsYC0GKrSv_vd94i_jqOc95iXvtUm26B96rBfFYhy0130_provenance {
  dgn-np:NP75158.RA3MsYC0GKrSv_vd94i_jqOc95iXvtUm26B96rBfFYhy0130_assertion dcterms:description
      "[Our results indicated that the factor V Leiden and prothrombin G20210A mutations are not rare among populations of Western Iran and that the relationship between venous thrombophilia and these mutations have to be further studied in Western Iran population, which, in turn, may suggest a causal effect.]. 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:17700999;
    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:NP75158.RA3MsYC0GKrSv_vd94i_jqOc95iXvtUm26B96rBfFYhy0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:36+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" .
}