@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP58414.RAdkghBnkZumEFnHRADtiYVT7wTOKsYO5JfsH8XdF9vsw> .
@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:NP58414.RAdkghBnkZumEFnHRADtiYVT7wTOKsYO5JfsH8XdF9vsw130_head {
  this: np:hasAssertion dgn-np:NP58414.RAdkghBnkZumEFnHRADtiYVT7wTOKsYO5JfsH8XdF9vsw130_assertion;
    np:hasProvenance dgn-np:NP58414.RAdkghBnkZumEFnHRADtiYVT7wTOKsYO5JfsH8XdF9vsw130_provenance;
    np:hasPublicationInfo dgn-np:NP58414.RAdkghBnkZumEFnHRADtiYVT7wTOKsYO5JfsH8XdF9vsw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP58414.RAdkghBnkZumEFnHRADtiYVT7wTOKsYO5JfsH8XdF9vsw130_assertion a np:Assertion .
  
  dgn-np:NP58414.RAdkghBnkZumEFnHRADtiYVT7wTOKsYO5JfsH8XdF9vsw130_provenance a np:Provenance .
  
  dgn-np:NP58414.RAdkghBnkZumEFnHRADtiYVT7wTOKsYO5JfsH8XdF9vsw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP58414.RAdkghBnkZumEFnHRADtiYVT7wTOKsYO5JfsH8XdF9vsw130_assertion {
  miriam-gene:3105 a ncit:C16612 .
  
  lld:C0024299 a ncit:C7057 .
  
  dgn-gda:DGN3f88c75f420fffd23f98b0acda26c79d sio:SIO_000628 miriam-gene:3105, lld:C0024299;
    a sio:SIO_001122 .
}

dgn-np:NP58414.RAdkghBnkZumEFnHRADtiYVT7wTOKsYO5JfsH8XdF9vsw130_provenance {
  dgn-np:NP58414.RAdkghBnkZumEFnHRADtiYVT7wTOKsYO5JfsH8XdF9vsw130_assertion dcterms:description
      "[These data can be used as control data for HLA disease associations and paternity studies, but they are also important for the evaluation of the probability rate of success in determining the optimal matched donor in unrelated stem transplantation for Tunisian patients or patients of Tunisian origin.]. 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:15361135;
    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:NP58414.RAdkghBnkZumEFnHRADtiYVT7wTOKsYO5JfsH8XdF9vsw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:27+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" .
}