@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP785914.RAXl4Wbyl7IzivBrwOC-LHiKM5efPZaJs08Ji7W8Sd4DY> .
@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:NP785914.RAXl4Wbyl7IzivBrwOC-LHiKM5efPZaJs08Ji7W8Sd4DY130_head {
  this: np:hasAssertion dgn-np:NP785914.RAXl4Wbyl7IzivBrwOC-LHiKM5efPZaJs08Ji7W8Sd4DY130_assertion;
    np:hasProvenance dgn-np:NP785914.RAXl4Wbyl7IzivBrwOC-LHiKM5efPZaJs08Ji7W8Sd4DY130_provenance;
    np:hasPublicationInfo dgn-np:NP785914.RAXl4Wbyl7IzivBrwOC-LHiKM5efPZaJs08Ji7W8Sd4DY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP785914.RAXl4Wbyl7IzivBrwOC-LHiKM5efPZaJs08Ji7W8Sd4DY130_assertion a np:Assertion .
  
  dgn-np:NP785914.RAXl4Wbyl7IzivBrwOC-LHiKM5efPZaJs08Ji7W8Sd4DY130_provenance a np:Provenance .
  
  dgn-np:NP785914.RAXl4Wbyl7IzivBrwOC-LHiKM5efPZaJs08Ji7W8Sd4DY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP785914.RAXl4Wbyl7IzivBrwOC-LHiKM5efPZaJs08Ji7W8Sd4DY130_assertion {
  miriam-gene:2153 a ncit:C16612 .
  
  lld:C0011849 a ncit:C7057 .
  
  dgn-gda:DGN3a7d37e41a6ccd29c197aaa3bab190e2 sio:SIO_000628 miriam-gene:2153, lld:C0011849;
    a sio:SIO_001121 .
}

dgn-np:NP785914.RAXl4Wbyl7IzivBrwOC-LHiKM5efPZaJs08Ji7W8Sd4DY130_provenance {
  dgn-np:NP785914.RAXl4Wbyl7IzivBrwOC-LHiKM5efPZaJs08Ji7W8Sd4DY130_assertion dcterms:description
      "[There were no significant differences in terms of diabetes mellitus, hypertension, dyslipidemia, plasma fibrinogen level, smoking, gender and family history of CAD with and without the FVL mutation in the patient group.]. 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:17982311;
    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:NP785914.RAXl4Wbyl7IzivBrwOC-LHiKM5efPZaJs08Ji7W8Sd4DY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:56+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" .
}