@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP66325.RAgyJhp2ksScnGxpz3plBkB8epFXHgP4zSYztBZjCMsAo> .
@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:NP66325.RAgyJhp2ksScnGxpz3plBkB8epFXHgP4zSYztBZjCMsAo130_head {
  this: np:hasAssertion dgn-np:NP66325.RAgyJhp2ksScnGxpz3plBkB8epFXHgP4zSYztBZjCMsAo130_assertion;
    np:hasProvenance dgn-np:NP66325.RAgyJhp2ksScnGxpz3plBkB8epFXHgP4zSYztBZjCMsAo130_provenance;
    np:hasPublicationInfo dgn-np:NP66325.RAgyJhp2ksScnGxpz3plBkB8epFXHgP4zSYztBZjCMsAo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP66325.RAgyJhp2ksScnGxpz3plBkB8epFXHgP4zSYztBZjCMsAo130_assertion a np:Assertion .
  
  dgn-np:NP66325.RAgyJhp2ksScnGxpz3plBkB8epFXHgP4zSYztBZjCMsAo130_provenance a np:Provenance .
  
  dgn-np:NP66325.RAgyJhp2ksScnGxpz3plBkB8epFXHgP4zSYztBZjCMsAo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP66325.RAgyJhp2ksScnGxpz3plBkB8epFXHgP4zSYztBZjCMsAo130_assertion {
  miriam-gene:10544 a ncit:C16612 .
  
  lld:C0038454 a ncit:C7057 .
  
  dgn-gda:DGN1a004e2120ff35ca78076439dc4b04a1 sio:SIO_000628 miriam-gene:10544, lld:C0038454;
    a sio:SIO_001122 .
}

dgn-np:NP66325.RAgyJhp2ksScnGxpz3plBkB8epFXHgP4zSYztBZjCMsAo130_provenance {
  dgn-np:NP66325.RAgyJhp2ksScnGxpz3plBkB8epFXHgP4zSYztBZjCMsAo130_assertion dcterms:description
      "[None of the patients with sEPCR levels below 100 ng/ml carried the A3 haplotype, while patients with elevated sEPCR levels carried the A3 haplotype either in a heterozygous or homozygous state. Our study confirms that there is a strong association between A3 haplotype and elevated sEPCR levels. We suggest that elevated sEPCR levels might increase the risk of stroke at pediatric age when compared to controls. Studies with large series of patients are warranted to confirm this hypothesis.]. 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:17027065;
    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:NP66325.RAgyJhp2ksScnGxpz3plBkB8epFXHgP4zSYztBZjCMsAo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:31+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" .
}