@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP420523.RAIZ-pIqzJXOJWLUI_TO2EHdd6idJUe4wwb333J8tR9Qo> .
@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:NP420523.RAIZ-pIqzJXOJWLUI_TO2EHdd6idJUe4wwb333J8tR9Qo130_head {
   this: np:hasAssertion dgn-np:NP420523.RAIZ-pIqzJXOJWLUI_TO2EHdd6idJUe4wwb333J8tR9Qo130_assertion ;
    np:hasProvenance dgn-np:NP420523.RAIZ-pIqzJXOJWLUI_TO2EHdd6idJUe4wwb333J8tR9Qo130_provenance ;
    np:hasPublicationInfo dgn-np:NP420523.RAIZ-pIqzJXOJWLUI_TO2EHdd6idJUe4wwb333J8tR9Qo130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP420523.RAIZ-pIqzJXOJWLUI_TO2EHdd6idJUe4wwb333J8tR9Qo130_assertion a np:Assertion .
  dgn-np:NP420523.RAIZ-pIqzJXOJWLUI_TO2EHdd6idJUe4wwb333J8tR9Qo130_provenance a np:Provenance .
  dgn-np:NP420523.RAIZ-pIqzJXOJWLUI_TO2EHdd6idJUe4wwb333J8tR9Qo130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP420523.RAIZ-pIqzJXOJWLUI_TO2EHdd6idJUe4wwb333J8tR9Qo130_assertion {
   miriam-gene:5660 a ncit:C16612 .
  lld:C0018799 a ncit:C7057 .
  dgn-gda:DGNfd37bdcc305319df27b9514d76434ecd sio:SIO_000628 miriam-gene:5660 , lld:C0018799 ;
    a sio:SIO_001121 .
}
dgn-np:NP420523.RAIZ-pIqzJXOJWLUI_TO2EHdd6idJUe4wwb333J8tR9Qo130_provenance {
   dgn-np:NP420523.RAIZ-pIqzJXOJWLUI_TO2EHdd6idJUe4wwb333J8tR9Qo130_assertion dcterms:description "[Numerous predisposing risk factors can be both inherited and acquired, including cardiac disease, vascular abnormalities, infectious diseases, collagen tissue diseases, inborn errors of metabolism, anticardiolipin antibody, lupus anticoagulant, deficiencies of protein C, protein S, antithrombin, or plasminogen, and prothrombotic mutations.]. 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:22759687 ;
    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:NP420523.RAIZ-pIqzJXOJWLUI_TO2EHdd6idJUe4wwb333J8tR9Qo130_publicationInfo {
   this: dcterms:created "2014-10-02T12:36:09+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" .
}