@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP389626.RAttCSpTWnenGSQVxSP-b5k0k-tSZZHDmfenUNTe7sVUE> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP389626.RAttCSpTWnenGSQVxSP-b5k0k-tSZZHDmfenUNTe7sVUE130_head {
  this: np:hasAssertion dgn-np:NP389626.RAttCSpTWnenGSQVxSP-b5k0k-tSZZHDmfenUNTe7sVUE130_assertion;
    np:hasProvenance dgn-np:NP389626.RAttCSpTWnenGSQVxSP-b5k0k-tSZZHDmfenUNTe7sVUE130_provenance;
    np:hasPublicationInfo dgn-np:NP389626.RAttCSpTWnenGSQVxSP-b5k0k-tSZZHDmfenUNTe7sVUE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP389626.RAttCSpTWnenGSQVxSP-b5k0k-tSZZHDmfenUNTe7sVUE130_assertion a np:Assertion .
  
  dgn-np:NP389626.RAttCSpTWnenGSQVxSP-b5k0k-tSZZHDmfenUNTe7sVUE130_provenance a np:Provenance .
  
  dgn-np:NP389626.RAttCSpTWnenGSQVxSP-b5k0k-tSZZHDmfenUNTe7sVUE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP389626.RAttCSpTWnenGSQVxSP-b5k0k-tSZZHDmfenUNTe7sVUE130_assertion {
  miriam-gene:2147 a ncit:C16612 .
  
  lld:C0155626 a ncit:C7057 .
  
  dgn-gda:DGNb989e527bc28e6937d709c7ac43bec56 sio:SIO_000628 miriam-gene:2147, lld:C0155626;
    a sio:SIO_001122 .
}

dgn-np:NP389626.RAttCSpTWnenGSQVxSP-b5k0k-tSZZHDmfenUNTe7sVUE130_provenance {
  dgn-np:NP389626.RAttCSpTWnenGSQVxSP-b5k0k-tSZZHDmfenUNTe7sVUE130_assertion dcterms:description
      "[In all the studies we examined, the polymorphism G20210A in the prothrombin gene was associated with an increased risk of acute myocardial infarction (AMI) in young people, especially when other risk factors were present.]. 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:15284679;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP389626.RAttCSpTWnenGSQVxSP-b5k0k-tSZZHDmfenUNTe7sVUE130_publicationInfo {
  this: dcterms:created "2015-08-25T14:41:25+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}