@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP909315.RAz8bG0sqfS0ci4HX3J1CERAk2WBxtZDlCk1305_Ts94A> .
@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:NP909315.RAz8bG0sqfS0ci4HX3J1CERAk2WBxtZDlCk1305_Ts94A130_head {
  this: np:hasAssertion dgn-np:NP909315.RAz8bG0sqfS0ci4HX3J1CERAk2WBxtZDlCk1305_Ts94A130_assertion;
    np:hasProvenance dgn-np:NP909315.RAz8bG0sqfS0ci4HX3J1CERAk2WBxtZDlCk1305_Ts94A130_provenance;
    np:hasPublicationInfo dgn-np:NP909315.RAz8bG0sqfS0ci4HX3J1CERAk2WBxtZDlCk1305_Ts94A130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP909315.RAz8bG0sqfS0ci4HX3J1CERAk2WBxtZDlCk1305_Ts94A130_assertion a np:Assertion .
  
  dgn-np:NP909315.RAz8bG0sqfS0ci4HX3J1CERAk2WBxtZDlCk1305_Ts94A130_provenance a np:Provenance .
  
  dgn-np:NP909315.RAz8bG0sqfS0ci4HX3J1CERAk2WBxtZDlCk1305_Ts94A130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP909315.RAz8bG0sqfS0ci4HX3J1CERAk2WBxtZDlCk1305_Ts94A130_assertion {
  miriam-gene:1280 a ncit:C16612 .
  
  lld:C0398623 a ncit:C7057 .
  
  dgn-gda:DGN540bab9112981c9faa92643009b50531 sio:SIO_000628 miriam-gene:1280, lld:C0398623;
    a sio:SIO_001121 .
}

dgn-np:NP909315.RAz8bG0sqfS0ci4HX3J1CERAk2WBxtZDlCk1305_Ts94A130_provenance {
  dgn-np:NP909315.RAz8bG0sqfS0ci4HX3J1CERAk2WBxtZDlCk1305_Ts94A130_assertion dcterms:description
      "[The etiology of ANFH is unknown, but previous studies have indicated that heritable thrombophilia (increased tendency to form thrombi) and hypofibrinolysis (reduced ability to lyse thrombi), alcohol intake, and steroid use are risk factors for ANFH.]. 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:15179599;
    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:NP909315.RAz8bG0sqfS0ci4HX3J1CERAk2WBxtZDlCk1305_Ts94A130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:18+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" .
}