@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP44399.RApz3a6X80OO6cfQ7fNBvDcHFhSchcKHjq1X0ztwLuP-Q> .
@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:NP44399.RApz3a6X80OO6cfQ7fNBvDcHFhSchcKHjq1X0ztwLuP-Q130_head {
  this: np:hasAssertion dgn-np:NP44399.RApz3a6X80OO6cfQ7fNBvDcHFhSchcKHjq1X0ztwLuP-Q130_assertion;
    np:hasProvenance dgn-np:NP44399.RApz3a6X80OO6cfQ7fNBvDcHFhSchcKHjq1X0ztwLuP-Q130_provenance;
    np:hasPublicationInfo dgn-np:NP44399.RApz3a6X80OO6cfQ7fNBvDcHFhSchcKHjq1X0ztwLuP-Q130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP44399.RApz3a6X80OO6cfQ7fNBvDcHFhSchcKHjq1X0ztwLuP-Q130_assertion a np:Assertion .
  
  dgn-np:NP44399.RApz3a6X80OO6cfQ7fNBvDcHFhSchcKHjq1X0ztwLuP-Q130_provenance a np:Provenance .
  
  dgn-np:NP44399.RApz3a6X80OO6cfQ7fNBvDcHFhSchcKHjq1X0ztwLuP-Q130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP44399.RApz3a6X80OO6cfQ7fNBvDcHFhSchcKHjq1X0ztwLuP-Q130_assertion {
  miriam-gene:2153 a ncit:C16612 .
  
  lld:C0027051 a ncit:C7057 .
  
  dgn-gda:DGNc25c3b41e0960cbfc0ac1f58884a6101 sio:SIO_000628 miriam-gene:2153, lld:C0027051;
    a sio:SIO_001122 .
}

dgn-np:NP44399.RApz3a6X80OO6cfQ7fNBvDcHFhSchcKHjq1X0ztwLuP-Q130_provenance {
  dgn-np:NP44399.RApz3a6X80OO6cfQ7fNBvDcHFhSchcKHjq1X0ztwLuP-Q130_assertion dct:description
      "[In a large cohort of young AMI patients the gain-of-function variant F5 G1691A was associated with an increased risk of AMI. The findings on the variant F2 G20210A confirmed the previously reported results, but the association was statistically not significant. These data suggest that a number of young patients with AMI carry gene variants associated with a procoagulant phenotype.]. 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:20626623;
    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:NP44399.RApz3a6X80OO6cfQ7fNBvDcHFhSchcKHjq1X0ztwLuP-Q130_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" .
}