@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP55944.RAb0UL0hOnMyLjyYDkJRKEs1Zh0mCryHEtEaqlThKZvZE> .
@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:NP55944.RAb0UL0hOnMyLjyYDkJRKEs1Zh0mCryHEtEaqlThKZvZE130_head {
  this: np:hasAssertion dgn-np:NP55944.RAb0UL0hOnMyLjyYDkJRKEs1Zh0mCryHEtEaqlThKZvZE130_assertion;
    np:hasProvenance dgn-np:NP55944.RAb0UL0hOnMyLjyYDkJRKEs1Zh0mCryHEtEaqlThKZvZE130_provenance;
    np:hasPublicationInfo dgn-np:NP55944.RAb0UL0hOnMyLjyYDkJRKEs1Zh0mCryHEtEaqlThKZvZE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP55944.RAb0UL0hOnMyLjyYDkJRKEs1Zh0mCryHEtEaqlThKZvZE130_assertion a np:Assertion .
  
  dgn-np:NP55944.RAb0UL0hOnMyLjyYDkJRKEs1Zh0mCryHEtEaqlThKZvZE130_provenance a np:Provenance .
  
  dgn-np:NP55944.RAb0UL0hOnMyLjyYDkJRKEs1Zh0mCryHEtEaqlThKZvZE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP55944.RAb0UL0hOnMyLjyYDkJRKEs1Zh0mCryHEtEaqlThKZvZE130_assertion {
  miriam-gene:3578 a ncit:C16612 .
  
  lld:C0007570 a ncit:C7057 .
  
  dgn-gda:DGN50a66ba80864b3fddd0004b6a68af4c9 sio:SIO_000628 miriam-gene:3578, lld:C0007570;
    a sio:SIO_001122 .
}

dgn-np:NP55944.RAb0UL0hOnMyLjyYDkJRKEs1Zh0mCryHEtEaqlThKZvZE130_provenance {
  dgn-np:NP55944.RAb0UL0hOnMyLjyYDkJRKEs1Zh0mCryHEtEaqlThKZvZE130_assertion dcterms:description
      "[There were no statistically significant allele or haplotype frequency differences between cases and controls. Therefore, these results provide no evidence that these loci are associated with CD in this sample population.]. 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:15713213;
    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:NP55944.RAb0UL0hOnMyLjyYDkJRKEs1Zh0mCryHEtEaqlThKZvZE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:26+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" .
}