@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP501283.RAIEQxG5p7yYMQoRBT8hFbee0V99HDZquMANEXEJs2Wp0> .
@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:NP501283.RAIEQxG5p7yYMQoRBT8hFbee0V99HDZquMANEXEJs2Wp0130_head {
  this: np:hasAssertion dgn-np:NP501283.RAIEQxG5p7yYMQoRBT8hFbee0V99HDZquMANEXEJs2Wp0130_assertion;
    np:hasProvenance dgn-np:NP501283.RAIEQxG5p7yYMQoRBT8hFbee0V99HDZquMANEXEJs2Wp0130_provenance;
    np:hasPublicationInfo dgn-np:NP501283.RAIEQxG5p7yYMQoRBT8hFbee0V99HDZquMANEXEJs2Wp0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP501283.RAIEQxG5p7yYMQoRBT8hFbee0V99HDZquMANEXEJs2Wp0130_assertion a np:Assertion .
  
  dgn-np:NP501283.RAIEQxG5p7yYMQoRBT8hFbee0V99HDZquMANEXEJs2Wp0130_provenance a np:Provenance .
  
  dgn-np:NP501283.RAIEQxG5p7yYMQoRBT8hFbee0V99HDZquMANEXEJs2Wp0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP501283.RAIEQxG5p7yYMQoRBT8hFbee0V99HDZquMANEXEJs2Wp0130_assertion {
  miriam-gene:1082 a ncit:C16612 .
  
  lld:C0162739 a ncit:C7057 .
  
  dgn-gda:DGN6b078a3d58427ab7493c94cb8ff2b55c sio:SIO_000628 miriam-gene:1082, lld:C0162739;
    a sio:SIO_001121 .
}

dgn-np:NP501283.RAIEQxG5p7yYMQoRBT8hFbee0V99HDZquMANEXEJs2Wp0130_provenance {
  dgn-np:NP501283.RAIEQxG5p7yYMQoRBT8hFbee0V99HDZquMANEXEJs2Wp0130_assertion dcterms:description
      "[Out of the 350 differentially expressed genes in preeclampsia and 554 genes in HELLP syndrome, 224 genes (including LEP, CGB, LHB, INHA, SIGLEC6, PAPPA2, TREM1, and FLT1) changed in the same direction (elevated or reduced) in both syndromes.]. 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:20541258;
    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:NP501283.RAIEQxG5p7yYMQoRBT8hFbee0V99HDZquMANEXEJs2Wp0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:59+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" .
}