@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP793449.RAEL28GruUCQn7ZLayXdr4b-YV9sR7b2CmXiFuSYVLPqU> .
@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:NP793449.RAEL28GruUCQn7ZLayXdr4b-YV9sR7b2CmXiFuSYVLPqU130_head {
  this: np:hasAssertion dgn-np:NP793449.RAEL28GruUCQn7ZLayXdr4b-YV9sR7b2CmXiFuSYVLPqU130_assertion;
    np:hasProvenance dgn-np:NP793449.RAEL28GruUCQn7ZLayXdr4b-YV9sR7b2CmXiFuSYVLPqU130_provenance;
    np:hasPublicationInfo dgn-np:NP793449.RAEL28GruUCQn7ZLayXdr4b-YV9sR7b2CmXiFuSYVLPqU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP793449.RAEL28GruUCQn7ZLayXdr4b-YV9sR7b2CmXiFuSYVLPqU130_assertion a np:Assertion .
  
  dgn-np:NP793449.RAEL28GruUCQn7ZLayXdr4b-YV9sR7b2CmXiFuSYVLPqU130_provenance a np:Provenance .
  
  dgn-np:NP793449.RAEL28GruUCQn7ZLayXdr4b-YV9sR7b2CmXiFuSYVLPqU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP793449.RAEL28GruUCQn7ZLayXdr4b-YV9sR7b2CmXiFuSYVLPqU130_assertion {
  miriam-gene:5624 a ncit:C16612 .
  
  lld:C0040038 a ncit:C7057 .
  
  dgn-gda:DGN1435a537cad8cf7855f716d898bec7d5 sio:SIO_000628 miriam-gene:5624, lld:C0040038;
    a sio:SIO_001121 .
}

dgn-np:NP793449.RAEL28GruUCQn7ZLayXdr4b-YV9sR7b2CmXiFuSYVLPqU130_provenance {
  dgn-np:NP793449.RAEL28GruUCQn7ZLayXdr4b-YV9sR7b2CmXiFuSYVLPqU130_assertion dcterms:description
      "[Here we have analysed 125 consecutive patients with incidental or recurrent venous thromboembolism for the presence of mutations at the cleavage sites for APC at amino acid positions Arg336 and Arg562 of factor VIII.]. 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:8616046;
    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:NP793449.RAEL28GruUCQn7ZLayXdr4b-YV9sR7b2CmXiFuSYVLPqU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:07+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" .
}