@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP216617.RAsFzDKSMZbC2sSdghnGmMweKwF0Jp1wgbmpgtN34aOgs> .
@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:NP216617.RAsFzDKSMZbC2sSdghnGmMweKwF0Jp1wgbmpgtN34aOgs130_head {
  this: np:hasAssertion dgn-np:NP216617.RAsFzDKSMZbC2sSdghnGmMweKwF0Jp1wgbmpgtN34aOgs130_assertion ;
    np:hasProvenance dgn-np:NP216617.RAsFzDKSMZbC2sSdghnGmMweKwF0Jp1wgbmpgtN34aOgs130_provenance ;
    np:hasPublicationInfo dgn-np:NP216617.RAsFzDKSMZbC2sSdghnGmMweKwF0Jp1wgbmpgtN34aOgs130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP216617.RAsFzDKSMZbC2sSdghnGmMweKwF0Jp1wgbmpgtN34aOgs130_assertion a np:Assertion .
  dgn-np:NP216617.RAsFzDKSMZbC2sSdghnGmMweKwF0Jp1wgbmpgtN34aOgs130_provenance a np:Provenance .
  dgn-np:NP216617.RAsFzDKSMZbC2sSdghnGmMweKwF0Jp1wgbmpgtN34aOgs130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP216617.RAsFzDKSMZbC2sSdghnGmMweKwF0Jp1wgbmpgtN34aOgs130_assertion {
  miriam-gene:5555 a ncit:C16612 .
  lld:C0398623 a ncit:C7057 .
  dgn-gda:DGN648e9fb54eef25f1689ca2f9abb40c40 sio:SIO_000628 miriam-gene:5555 , lld:C0398623 ;
    a sio:SIO_001121 .
}
dgn-np:NP216617.RAsFzDKSMZbC2sSdghnGmMweKwF0Jp1wgbmpgtN34aOgs130_provenance {
  dgn-np:NP216617.RAsFzDKSMZbC2sSdghnGmMweKwF0Jp1wgbmpgtN34aOgs130_assertion dcterms:description "[Acquired causes include conditions such as surgery, cancer, and prolonged immobilization, while genetic causes have been linked to the inherited deficiencies of antithrombin, protein C, and protein S. The identification of the genetic basis of these inherited causes of thrombophilia ushered in a new way of thinking about thrombosis and the importance of its genetic component.]. 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:16315746 ;
    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:NP216617.RAsFzDKSMZbC2sSdghnGmMweKwF0Jp1wgbmpgtN34aOgs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:00+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" .
}