@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP516107.RAcYhT6gqz0_fdte30sFI9aRJxHa62tBhcTb414PLq6qg> .
@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:NP516107.RAcYhT6gqz0_fdte30sFI9aRJxHa62tBhcTb414PLq6qg130_head {
  this: np:hasAssertion dgn-np:NP516107.RAcYhT6gqz0_fdte30sFI9aRJxHa62tBhcTb414PLq6qg130_assertion;
    np:hasProvenance dgn-np:NP516107.RAcYhT6gqz0_fdte30sFI9aRJxHa62tBhcTb414PLq6qg130_provenance;
    np:hasPublicationInfo dgn-np:NP516107.RAcYhT6gqz0_fdte30sFI9aRJxHa62tBhcTb414PLq6qg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP516107.RAcYhT6gqz0_fdte30sFI9aRJxHa62tBhcTb414PLq6qg130_assertion a np:Assertion .
  
  dgn-np:NP516107.RAcYhT6gqz0_fdte30sFI9aRJxHa62tBhcTb414PLq6qg130_provenance a np:Provenance .
  
  dgn-np:NP516107.RAcYhT6gqz0_fdte30sFI9aRJxHa62tBhcTb414PLq6qg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP516107.RAcYhT6gqz0_fdte30sFI9aRJxHa62tBhcTb414PLq6qg130_assertion {
  miriam-gene:4524 a ncit:C16612 .
  
  lld:C1260403 a ncit:C7057 .
  
  dgn-gda:DGNb50b8b556e5cbcb809ec577fa8d5bb12 sio:SIO_000628 miriam-gene:4524, lld:C1260403;
    a sio:SIO_001121 .
}

dgn-np:NP516107.RAcYhT6gqz0_fdte30sFI9aRJxHa62tBhcTb414PLq6qg130_provenance {
  dgn-np:NP516107.RAcYhT6gqz0_fdte30sFI9aRJxHa62tBhcTb414PLq6qg130_assertion dcterms:description
      "[If the cause of thrombosis cannot be explained by the usual factors attributed to the occurrence of thrombosis in NS, screening for the other factors, such as FVL, MTHFR, and prothrombin gene mutation, may be beneficial.]. 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:23458174;
    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:NP516107.RAcYhT6gqz0_fdte30sFI9aRJxHa62tBhcTb414PLq6qg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:07+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" .
}