@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP365007.RAB4Kmv_sV8RM-YcDUWBMMMT2OVgT18n1EPoMFe9dhv2A> .
@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 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:NP365007.RAB4Kmv_sV8RM-YcDUWBMMMT2OVgT18n1EPoMFe9dhv2A130_head {
  this: np:hasAssertion dgn-np:NP365007.RAB4Kmv_sV8RM-YcDUWBMMMT2OVgT18n1EPoMFe9dhv2A130_assertion;
    np:hasProvenance dgn-np:NP365007.RAB4Kmv_sV8RM-YcDUWBMMMT2OVgT18n1EPoMFe9dhv2A130_provenance;
    np:hasPublicationInfo dgn-np:NP365007.RAB4Kmv_sV8RM-YcDUWBMMMT2OVgT18n1EPoMFe9dhv2A130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP365007.RAB4Kmv_sV8RM-YcDUWBMMMT2OVgT18n1EPoMFe9dhv2A130_assertion a np:Assertion .
  
  dgn-np:NP365007.RAB4Kmv_sV8RM-YcDUWBMMMT2OVgT18n1EPoMFe9dhv2A130_provenance a np:Provenance .
  
  dgn-np:NP365007.RAB4Kmv_sV8RM-YcDUWBMMMT2OVgT18n1EPoMFe9dhv2A130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP365007.RAB4Kmv_sV8RM-YcDUWBMMMT2OVgT18n1EPoMFe9dhv2A130_assertion {
  miriam-gene:6007 a ncit:C16612 .
  
  lld:C0014761 a ncit:C7057 .
  
  dgn-gda:DGN94d176aeb768c98b7ddcaf277595c5f0 sio:SIO_000628 miriam-gene:6007, lld:C0014761;
    a sio:SIO_001121 .
}

dgn-np:NP365007.RAB4Kmv_sV8RM-YcDUWBMMMT2OVgT18n1EPoMFe9dhv2A130_provenance {
  dgn-np:NP365007.RAB4Kmv_sV8RM-YcDUWBMMMT2OVgT18n1EPoMFe9dhv2A130_assertion dct: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: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:NP365007.RAB4Kmv_sV8RM-YcDUWBMMMT2OVgT18n1EPoMFe9dhv2A130_publicationInfo {
  this: dct:created "2014-10-02T12:35:33+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}