@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP524885.RAaFWt-rMy56brx5sTslrMDmnS38VXM_IrSdbVN-F6otk> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP524885.RAaFWt-rMy56brx5sTslrMDmnS38VXM_IrSdbVN-F6otk130_head {
  this: np:hasAssertion dgn-np:NP524885.RAaFWt-rMy56brx5sTslrMDmnS38VXM_IrSdbVN-F6otk130_assertion;
    np:hasProvenance dgn-np:NP524885.RAaFWt-rMy56brx5sTslrMDmnS38VXM_IrSdbVN-F6otk130_provenance;
    np:hasPublicationInfo dgn-np:NP524885.RAaFWt-rMy56brx5sTslrMDmnS38VXM_IrSdbVN-F6otk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP524885.RAaFWt-rMy56brx5sTslrMDmnS38VXM_IrSdbVN-F6otk130_assertion a np:Assertion .
  
  dgn-np:NP524885.RAaFWt-rMy56brx5sTslrMDmnS38VXM_IrSdbVN-F6otk130_provenance a np:Provenance .
  
  dgn-np:NP524885.RAaFWt-rMy56brx5sTslrMDmnS38VXM_IrSdbVN-F6otk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP524885.RAaFWt-rMy56brx5sTslrMDmnS38VXM_IrSdbVN-F6otk130_assertion {
  miriam-gene:3813 a ncit:C16612 .
  
  lld:C0011854 a ncit:C7057 .
  
  dgn-gda:DGNde88b2705fd22aead5112e44372a268a sio:SIO_000628 miriam-gene:3813, lld:C0011854;
    a sio:SIO_001121 .
}

dgn-np:NP524885.RAaFWt-rMy56brx5sTslrMDmnS38VXM_IrSdbVN-F6otk130_provenance {
  dgn-np:NP524885.RAaFWt-rMy56brx5sTslrMDmnS38VXM_IrSdbVN-F6otk130_assertion dcterms:description
      "[We applied this method to assess copy number variation in two KIR genes, KIR3DL1 and KIR3DS1, which are suitable candidates for T1D susceptibility since they encode the only KIR molecules known to bind with HLA-Bw4 epitopes.]. 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:24720548;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP524885.RAaFWt-rMy56brx5sTslrMDmnS38VXM_IrSdbVN-F6otk130_publicationInfo {
  this: dcterms:created "2015-08-25T14:42:50+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}