@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP559216.RAsuQapR1WKfXO2i-aRrciRQnS3FwPAxKw2cki4pYMjsI> .
@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:NP559216.RAsuQapR1WKfXO2i-aRrciRQnS3FwPAxKw2cki4pYMjsI130_head {
  this: np:hasAssertion dgn-np:NP559216.RAsuQapR1WKfXO2i-aRrciRQnS3FwPAxKw2cki4pYMjsI130_assertion;
    np:hasProvenance dgn-np:NP559216.RAsuQapR1WKfXO2i-aRrciRQnS3FwPAxKw2cki4pYMjsI130_provenance;
    np:hasPublicationInfo dgn-np:NP559216.RAsuQapR1WKfXO2i-aRrciRQnS3FwPAxKw2cki4pYMjsI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP559216.RAsuQapR1WKfXO2i-aRrciRQnS3FwPAxKw2cki4pYMjsI130_assertion a np:Assertion .
  
  dgn-np:NP559216.RAsuQapR1WKfXO2i-aRrciRQnS3FwPAxKw2cki4pYMjsI130_provenance a np:Provenance .
  
  dgn-np:NP559216.RAsuQapR1WKfXO2i-aRrciRQnS3FwPAxKw2cki4pYMjsI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP559216.RAsuQapR1WKfXO2i-aRrciRQnS3FwPAxKw2cki4pYMjsI130_assertion {
  miriam-gene:30811 a ncit:C16612 .
  
  lld:C0020305 a ncit:C7057 .
  
  dgn-gda:DGNc13b4af46094881d36094e6ca776ec29 sio:SIO_000628 miriam-gene:30811, lld:C0020305;
    a sio:SIO_001121 .
}

dgn-np:NP559216.RAsuQapR1WKfXO2i-aRrciRQnS3FwPAxKw2cki4pYMjsI130_provenance {
  dgn-np:NP559216.RAsuQapR1WKfXO2i-aRrciRQnS3FwPAxKw2cki4pYMjsI130_assertion dcterms:description
      "[Disease outcomes of bone marrow failure in patients with high turnover of red blood cells and immunocompromised conditions, and fetal hydrops in pregnant women are resulted from the targeting and destruction of specifically erythroid progenitors of the human bone marrow by B19V.]. 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:21698228;
    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:NP559216.RAsuQapR1WKfXO2i-aRrciRQnS3FwPAxKw2cki4pYMjsI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:37+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" .
}