@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP44414.RAhqOtmyZ_KOzw5NhgIoiytiYD1Qz5YllZkozWunc2y4w> .
@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 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:NP44414.RAhqOtmyZ_KOzw5NhgIoiytiYD1Qz5YllZkozWunc2y4w130_head {
  this: np:hasAssertion dgn-np:NP44414.RAhqOtmyZ_KOzw5NhgIoiytiYD1Qz5YllZkozWunc2y4w130_assertion;
    np:hasProvenance dgn-np:NP44414.RAhqOtmyZ_KOzw5NhgIoiytiYD1Qz5YllZkozWunc2y4w130_provenance;
    np:hasPublicationInfo dgn-np:NP44414.RAhqOtmyZ_KOzw5NhgIoiytiYD1Qz5YllZkozWunc2y4w130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP44414.RAhqOtmyZ_KOzw5NhgIoiytiYD1Qz5YllZkozWunc2y4w130_assertion a np:Assertion .
  
  dgn-np:NP44414.RAhqOtmyZ_KOzw5NhgIoiytiYD1Qz5YllZkozWunc2y4w130_provenance a np:Provenance .
  
  dgn-np:NP44414.RAhqOtmyZ_KOzw5NhgIoiytiYD1Qz5YllZkozWunc2y4w130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP44414.RAhqOtmyZ_KOzw5NhgIoiytiYD1Qz5YllZkozWunc2y4w130_assertion {
  miriam-gene:2153 a ncit:C16612 .
  
  lld:C0010054 a ncit:C7057 .
  
  dgn-gda:DGNe29d4aba29d3bebc0a092bfedfed99f4 sio:SIO_000628 miriam-gene:2153, lld:C0010054;
    a sio:SIO_001122 .
}

dgn-np:NP44414.RAhqOtmyZ_KOzw5NhgIoiytiYD1Qz5YllZkozWunc2y4w130_provenance {
  dgn-np:NP44414.RAhqOtmyZ_KOzw5NhgIoiytiYD1Qz5YllZkozWunc2y4w130_assertion dct:description
      "[Since identification of genetic risk factors for CAD in different ethnic groups is important for the development of new intervention and prevention programs, we investigated the association between the R353Q and -323ins10 polymorphisms in Factor VII gene, C677T mutation in MTHFR, Factor V Leiden and PT G20210A mutations and CAD in Turkish population.]. 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:16472842;
    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:NP44414.RAhqOtmyZ_KOzw5NhgIoiytiYD1Qz5YllZkozWunc2y4w130_publicationInfo {
  this: dct:created "2014-10-02T12:32:20+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}