@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP61931.RAaxhoL-6P9MJd8bk-NwOnwRtrcYzfhO2B_md3o66kphY> .
@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:NP61931.RAaxhoL-6P9MJd8bk-NwOnwRtrcYzfhO2B_md3o66kphY130_head {
  this: np:hasAssertion dgn-np:NP61931.RAaxhoL-6P9MJd8bk-NwOnwRtrcYzfhO2B_md3o66kphY130_assertion;
    np:hasProvenance dgn-np:NP61931.RAaxhoL-6P9MJd8bk-NwOnwRtrcYzfhO2B_md3o66kphY130_provenance;
    np:hasPublicationInfo dgn-np:NP61931.RAaxhoL-6P9MJd8bk-NwOnwRtrcYzfhO2B_md3o66kphY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP61931.RAaxhoL-6P9MJd8bk-NwOnwRtrcYzfhO2B_md3o66kphY130_assertion a np:Assertion .
  
  dgn-np:NP61931.RAaxhoL-6P9MJd8bk-NwOnwRtrcYzfhO2B_md3o66kphY130_provenance a np:Provenance .
  
  dgn-np:NP61931.RAaxhoL-6P9MJd8bk-NwOnwRtrcYzfhO2B_md3o66kphY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP61931.RAaxhoL-6P9MJd8bk-NwOnwRtrcYzfhO2B_md3o66kphY130_assertion {
  miriam-gene:6007 a ncit:C16612 .
  
  lld:C0014761 a ncit:C7057 .
  
  dgn-gda:DGN17a4c3fe361e2df2827ef7d6ef40b111 sio:SIO_000628 miriam-gene:6007, lld:C0014761;
    a sio:SIO_001122 .
}

dgn-np:NP61931.RAaxhoL-6P9MJd8bk-NwOnwRtrcYzfhO2B_md3o66kphY130_provenance {
  dgn-np:NP61931.RAaxhoL-6P9MJd8bk-NwOnwRtrcYzfhO2B_md3o66kphY130_assertion dcterms:description
      "[ In a limited screen at the molecular level among 1000 random D+ donors in southwestern Germany, 20 donors were found carrying aberrant RHD alleles. Four of these alleles were new and likely sporadic. An estimate was derived of the variety that may be encountered in genotyping approaches, and it was concluded that even within the European population the variety of RHD alleles may be larger than anticipated.]. 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:15987365;
    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:NP61931.RAaxhoL-6P9MJd8bk-NwOnwRtrcYzfhO2B_md3o66kphY130_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" .
}