@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP61935.RAQz_wAF7uf2NNvaqmt3MEweXZKb1D9fMpUKo0OV0lkCg> .
@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:NP61935.RAQz_wAF7uf2NNvaqmt3MEweXZKb1D9fMpUKo0OV0lkCg130_head {
  this: np:hasAssertion dgn-np:NP61935.RAQz_wAF7uf2NNvaqmt3MEweXZKb1D9fMpUKo0OV0lkCg130_assertion;
    np:hasProvenance dgn-np:NP61935.RAQz_wAF7uf2NNvaqmt3MEweXZKb1D9fMpUKo0OV0lkCg130_provenance;
    np:hasPublicationInfo dgn-np:NP61935.RAQz_wAF7uf2NNvaqmt3MEweXZKb1D9fMpUKo0OV0lkCg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP61935.RAQz_wAF7uf2NNvaqmt3MEweXZKb1D9fMpUKo0OV0lkCg130_assertion a np:Assertion .
  
  dgn-np:NP61935.RAQz_wAF7uf2NNvaqmt3MEweXZKb1D9fMpUKo0OV0lkCg130_provenance a np:Provenance .
  
  dgn-np:NP61935.RAQz_wAF7uf2NNvaqmt3MEweXZKb1D9fMpUKo0OV0lkCg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP61935.RAQz_wAF7uf2NNvaqmt3MEweXZKb1D9fMpUKo0OV0lkCg130_assertion {
  miriam-gene:6007 a ncit:C16612 .
  
  lld:C0158962 a ncit:C7057 .
  
  dgn-gda:DGNd07bb7d55e869fa2f0529a66fcc3f9cf sio:SIO_000628 miriam-gene:6007, lld:C0158962;
    a sio:SIO_001122 .
}

dgn-np:NP61935.RAQz_wAF7uf2NNvaqmt3MEweXZKb1D9fMpUKo0OV0lkCg130_provenance {
  dgn-np:NP61935.RAQz_wAF7uf2NNvaqmt3MEweXZKb1D9fMpUKo0OV0lkCg130_assertion dcterms:description
      "[Use of the polymerase chain reaction (PCR) for detection of the RHD gene can measure the RHD gene status for unborn babies at risk for hemolytic disease of the newborn (HDN).]. 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:11288127;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP61935.RAQz_wAF7uf2NNvaqmt3MEweXZKb1D9fMpUKo0OV0lkCg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:29+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" .
}