@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP629495.RAZcuBwehKRtO7pKnRIeNXmOxkMqFlQcpPmbpflivbMbU> .
@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:NP629495.RAZcuBwehKRtO7pKnRIeNXmOxkMqFlQcpPmbpflivbMbU130_head {
  this: np:hasAssertion dgn-np:NP629495.RAZcuBwehKRtO7pKnRIeNXmOxkMqFlQcpPmbpflivbMbU130_assertion;
    np:hasProvenance dgn-np:NP629495.RAZcuBwehKRtO7pKnRIeNXmOxkMqFlQcpPmbpflivbMbU130_provenance;
    np:hasPublicationInfo dgn-np:NP629495.RAZcuBwehKRtO7pKnRIeNXmOxkMqFlQcpPmbpflivbMbU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP629495.RAZcuBwehKRtO7pKnRIeNXmOxkMqFlQcpPmbpflivbMbU130_assertion a np:Assertion .
  
  dgn-np:NP629495.RAZcuBwehKRtO7pKnRIeNXmOxkMqFlQcpPmbpflivbMbU130_provenance a np:Provenance .
  
  dgn-np:NP629495.RAZcuBwehKRtO7pKnRIeNXmOxkMqFlQcpPmbpflivbMbU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP629495.RAZcuBwehKRtO7pKnRIeNXmOxkMqFlQcpPmbpflivbMbU130_assertion {
  miriam-gene:356 a ncit:C16612 .
  
  lld:C0004364 a ncit:C7057 .
  
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dgn-np:NP629495.RAZcuBwehKRtO7pKnRIeNXmOxkMqFlQcpPmbpflivbMbU130_provenance {
  dgn-np:NP629495.RAZcuBwehKRtO7pKnRIeNXmOxkMqFlQcpPmbpflivbMbU130_assertion dcterms:description
      "[The presence of risk variants in complement regulatory proteins in patients with SLE and/or APL Ab who develop preeclampsia, as well as in preeclampsia patients lacking autoimmune disease, links complement activation to disease pathogenesis and suggests new targets for treatment of this important public health problem.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
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    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:NP629495.RAZcuBwehKRtO7pKnRIeNXmOxkMqFlQcpPmbpflivbMbU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:20+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;
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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" .
}