@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP177491.RAoZBZbA4_oAMj9snaLFsaZirs34cIlspeH5Ph-BavD9c> .
@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:NP177491.RAoZBZbA4_oAMj9snaLFsaZirs34cIlspeH5Ph-BavD9c130_head {
  this: np:hasAssertion dgn-np:NP177491.RAoZBZbA4_oAMj9snaLFsaZirs34cIlspeH5Ph-BavD9c130_assertion;
    np:hasProvenance dgn-np:NP177491.RAoZBZbA4_oAMj9snaLFsaZirs34cIlspeH5Ph-BavD9c130_provenance;
    np:hasPublicationInfo dgn-np:NP177491.RAoZBZbA4_oAMj9snaLFsaZirs34cIlspeH5Ph-BavD9c130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP177491.RAoZBZbA4_oAMj9snaLFsaZirs34cIlspeH5Ph-BavD9c130_assertion a np:Assertion .
  
  dgn-np:NP177491.RAoZBZbA4_oAMj9snaLFsaZirs34cIlspeH5Ph-BavD9c130_provenance a np:Provenance .
  
  dgn-np:NP177491.RAoZBZbA4_oAMj9snaLFsaZirs34cIlspeH5Ph-BavD9c130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP177491.RAoZBZbA4_oAMj9snaLFsaZirs34cIlspeH5Ph-BavD9c130_assertion {
  miriam-gene:11093 a ncit:C16612 .
  
  lld:C2717961 a ncit:C7057 .
  
  dgn-gda:DGN0b6becd08bb179a7ee3912ce3b42ed32 sio:SIO_000628 miriam-gene:11093, lld:C2717961;
    a sio:SIO_001121 .
}

dgn-np:NP177491.RAoZBZbA4_oAMj9snaLFsaZirs34cIlspeH5Ph-BavD9c130_provenance {
  dgn-np:NP177491.RAoZBZbA4_oAMj9snaLFsaZirs34cIlspeH5Ph-BavD9c130_assertion dcterms:description
      "[Diarrhea-negative HUS is associated with complement dysregulation in up to 50% of cases, caused by mutations in complement factor H, membrane cofactor protein, factor I or factor B, or by autoantibodies against factor H. The incomplete penetrance of mutations in either ADAMTS13 or complement regulatory genes suggests that precipitating events or triggers may be required to cause thrombotic microangiopathy in many patients.]. 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:18215115;
    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:NP177491.RAoZBZbA4_oAMj9snaLFsaZirs34cIlspeH5Ph-BavD9c130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:36+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" .
}