@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP266088.RAutyUvcTcT0tY0guAVbm7l2sD20Ry3WqJu3rGx1KmW0M> .
@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:NP266088.RAutyUvcTcT0tY0guAVbm7l2sD20Ry3WqJu3rGx1KmW0M130_head {
  this: np:hasAssertion dgn-np:NP266088.RAutyUvcTcT0tY0guAVbm7l2sD20Ry3WqJu3rGx1KmW0M130_assertion;
    np:hasProvenance dgn-np:NP266088.RAutyUvcTcT0tY0guAVbm7l2sD20Ry3WqJu3rGx1KmW0M130_provenance;
    np:hasPublicationInfo dgn-np:NP266088.RAutyUvcTcT0tY0guAVbm7l2sD20Ry3WqJu3rGx1KmW0M130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP266088.RAutyUvcTcT0tY0guAVbm7l2sD20Ry3WqJu3rGx1KmW0M130_assertion a np:Assertion .
  
  dgn-np:NP266088.RAutyUvcTcT0tY0guAVbm7l2sD20Ry3WqJu3rGx1KmW0M130_provenance a np:Provenance .
  
  dgn-np:NP266088.RAutyUvcTcT0tY0guAVbm7l2sD20Ry3WqJu3rGx1KmW0M130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP266088.RAutyUvcTcT0tY0guAVbm7l2sD20Ry3WqJu3rGx1KmW0M130_assertion {
  miriam-gene:5340 a ncit:C16612 .
  
  lld:C0398623 a ncit:C7057 .
  
  dgn-gda:DGN068bc3a34315bda71053c87eb1601778 sio:SIO_000628 miriam-gene:5340, lld:C0398623;
    a sio:SIO_001121 .
}

dgn-np:NP266088.RAutyUvcTcT0tY0guAVbm7l2sD20Ry3WqJu3rGx1KmW0M130_provenance {
  dgn-np:NP266088.RAutyUvcTcT0tY0guAVbm7l2sD20Ry3WqJu3rGx1KmW0M130_assertion dcterms:description
      "[The tests included in the second step of the screening are aimed at detecting the less common or less well established causes of inherited thrombophilia (low heparin cofactor II, defective release of tissue plasminogen activator, and high plasminogen activator inhibitor).]. 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:3116699;
    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:NP266088.RAutyUvcTcT0tY0guAVbm7l2sD20Ry3WqJu3rGx1KmW0M130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:28+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" .
}