@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP852095.RAtBl-93kYBAoWSVGQE0TrhGVnLZc64idJMMinPkTmoXo> .
@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:NP852095.RAtBl-93kYBAoWSVGQE0TrhGVnLZc64idJMMinPkTmoXo130_head {
  this: np:hasAssertion dgn-np:NP852095.RAtBl-93kYBAoWSVGQE0TrhGVnLZc64idJMMinPkTmoXo130_assertion;
    np:hasProvenance dgn-np:NP852095.RAtBl-93kYBAoWSVGQE0TrhGVnLZc64idJMMinPkTmoXo130_provenance;
    np:hasPublicationInfo dgn-np:NP852095.RAtBl-93kYBAoWSVGQE0TrhGVnLZc64idJMMinPkTmoXo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP852095.RAtBl-93kYBAoWSVGQE0TrhGVnLZc64idJMMinPkTmoXo130_assertion a np:Assertion .
  
  dgn-np:NP852095.RAtBl-93kYBAoWSVGQE0TrhGVnLZc64idJMMinPkTmoXo130_provenance a np:Provenance .
  
  dgn-np:NP852095.RAtBl-93kYBAoWSVGQE0TrhGVnLZc64idJMMinPkTmoXo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP852095.RAtBl-93kYBAoWSVGQE0TrhGVnLZc64idJMMinPkTmoXo130_assertion {
  miriam-gene:11093 a ncit:C16612 .
  
  lld:C0035078 a ncit:C7057 .
  
  dgn-gda:DGN148f8b96f43ce86f5b35625d765d8db1 sio:SIO_000628 miriam-gene:11093, lld:C0035078;
    a sio:SIO_001121 .
}

dgn-np:NP852095.RAtBl-93kYBAoWSVGQE0TrhGVnLZc64idJMMinPkTmoXo130_provenance {
  dgn-np:NP852095.RAtBl-93kYBAoWSVGQE0TrhGVnLZc64idJMMinPkTmoXo130_assertion dcterms:description
      "[Our experience appears to indicate the importance of assays of ADAMTS13 activity and its inhibitor in patients who have episodes of renal insufficiency in association with thrombotic microangiopathy, for diagnosis and choice of treatment.]. 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:16449289;
    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:NP852095.RAtBl-93kYBAoWSVGQE0TrhGVnLZc64idJMMinPkTmoXo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:40+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>,
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}