@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP443867.RAiiKhSU0XR30vCAXO9H7NqhqVV5QViKEohD-QUVaaK4k> .
@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:NP443867.RAiiKhSU0XR30vCAXO9H7NqhqVV5QViKEohD-QUVaaK4k130_head {
  this: np:hasAssertion dgn-np:NP443867.RAiiKhSU0XR30vCAXO9H7NqhqVV5QViKEohD-QUVaaK4k130_assertion;
    np:hasProvenance dgn-np:NP443867.RAiiKhSU0XR30vCAXO9H7NqhqVV5QViKEohD-QUVaaK4k130_provenance;
    np:hasPublicationInfo dgn-np:NP443867.RAiiKhSU0XR30vCAXO9H7NqhqVV5QViKEohD-QUVaaK4k130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP443867.RAiiKhSU0XR30vCAXO9H7NqhqVV5QViKEohD-QUVaaK4k130_assertion a np:Assertion .
  
  dgn-np:NP443867.RAiiKhSU0XR30vCAXO9H7NqhqVV5QViKEohD-QUVaaK4k130_provenance a np:Provenance .
  
  dgn-np:NP443867.RAiiKhSU0XR30vCAXO9H7NqhqVV5QViKEohD-QUVaaK4k130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP443867.RAiiKhSU0XR30vCAXO9H7NqhqVV5QViKEohD-QUVaaK4k130_assertion {
  miriam-gene:11214 a ncit:C16612 .
  
  lld:C0004153 a ncit:C7057 .
  
  dgn-gda:DGN4223138a5c0a1698bbd44ad85fc31318 sio:SIO_000628 miriam-gene:11214, lld:C0004153;
    a sio:SIO_001121 .
}

dgn-np:NP443867.RAiiKhSU0XR30vCAXO9H7NqhqVV5QViKEohD-QUVaaK4k130_provenance {
  dgn-np:NP443867.RAiiKhSU0XR30vCAXO9H7NqhqVV5QViKEohD-QUVaaK4k130_assertion dcterms:description
      "[The GWAS for aPTT was conducted in 9,240 individuals of European ancestry from the Atherosclerosis Risk in Communities (ARIC) study, and the GWAS for PT was conducted in 2,583 participants from the Genetic Study of Three Population Microisolates in South Tyrol (MICROS) and the Lothian Birth Cohorts (LBC) of 1921 and 1936.]. 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:22703881;
    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:NP443867.RAiiKhSU0XR30vCAXO9H7NqhqVV5QViKEohD-QUVaaK4k130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:24+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" .
}