@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP141232.RAejeq0bKYNG6LyL6S5EMoL99QHnww9MJ7r6WTr5oeUi8> .
@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:NP141232.RAejeq0bKYNG6LyL6S5EMoL99QHnww9MJ7r6WTr5oeUi8130_head {
  this: np:hasAssertion dgn-np:NP141232.RAejeq0bKYNG6LyL6S5EMoL99QHnww9MJ7r6WTr5oeUi8130_assertion;
    np:hasProvenance dgn-np:NP141232.RAejeq0bKYNG6LyL6S5EMoL99QHnww9MJ7r6WTr5oeUi8130_provenance;
    np:hasPublicationInfo dgn-np:NP141232.RAejeq0bKYNG6LyL6S5EMoL99QHnww9MJ7r6WTr5oeUi8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP141232.RAejeq0bKYNG6LyL6S5EMoL99QHnww9MJ7r6WTr5oeUi8130_assertion a np:Assertion .
  
  dgn-np:NP141232.RAejeq0bKYNG6LyL6S5EMoL99QHnww9MJ7r6WTr5oeUi8130_provenance a np:Provenance .
  
  dgn-np:NP141232.RAejeq0bKYNG6LyL6S5EMoL99QHnww9MJ7r6WTr5oeUi8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP141232.RAejeq0bKYNG6LyL6S5EMoL99QHnww9MJ7r6WTr5oeUi8130_assertion {
  miriam-gene:2147 a ncit:C16612 .
  
  lld:C0039082 a ncit:C7057 .
  
  dgn-gda:DGN47aa6b2d2a1a09781f8e68f9a8008faa sio:SIO_000628 miriam-gene:2147, lld:C0039082;
    a sio:SIO_001122 .
}

dgn-np:NP141232.RAejeq0bKYNG6LyL6S5EMoL99QHnww9MJ7r6WTr5oeUi8130_provenance {
  dgn-np:NP141232.RAejeq0bKYNG6LyL6S5EMoL99QHnww9MJ7r6WTr5oeUi8130_assertion dcterms:description
      "[These findings suggest that the 20210A prothrombin allele represents an inherited risk factor for acute coronary syndrome among patients who have limited extent of coronary disease at angiography or who lack major metabolic and acquired risk factors.]. 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:11741359;
    prov:wasDerivedFrom dgn-void:gad-20150221;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP141232.RAejeq0bKYNG6LyL6S5EMoL99QHnww9MJ7r6WTr5oeUi8130_publicationInfo {
  this: dcterms:created "2015-08-25T14:38:59+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" .
}