@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP842836.RAaDiicIsbaIdbttp0LOy6oy57tmRKWZyyAghZqChWMSg> .
@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:NP842836.RAaDiicIsbaIdbttp0LOy6oy57tmRKWZyyAghZqChWMSg130_head {
  this: np:hasAssertion dgn-np:NP842836.RAaDiicIsbaIdbttp0LOy6oy57tmRKWZyyAghZqChWMSg130_assertion;
    np:hasProvenance dgn-np:NP842836.RAaDiicIsbaIdbttp0LOy6oy57tmRKWZyyAghZqChWMSg130_provenance;
    np:hasPublicationInfo dgn-np:NP842836.RAaDiicIsbaIdbttp0LOy6oy57tmRKWZyyAghZqChWMSg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP842836.RAaDiicIsbaIdbttp0LOy6oy57tmRKWZyyAghZqChWMSg130_assertion a np:Assertion .
  
  dgn-np:NP842836.RAaDiicIsbaIdbttp0LOy6oy57tmRKWZyyAghZqChWMSg130_provenance a np:Provenance .
  
  dgn-np:NP842836.RAaDiicIsbaIdbttp0LOy6oy57tmRKWZyyAghZqChWMSg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP842836.RAaDiicIsbaIdbttp0LOy6oy57tmRKWZyyAghZqChWMSg130_assertion {
  miriam-gene:10085 a ncit:C16612 .
  
  lld:C0038013 a ncit:C7057 .
  
  dgn-gda:DGNdcfd0417c4025f6e8a22c884782610fb sio:SIO_000628 miriam-gene:10085, lld:C0038013;
    a sio:SIO_001121 .
}

dgn-np:NP842836.RAaDiicIsbaIdbttp0LOy6oy57tmRKWZyyAghZqChWMSg130_provenance {
  dgn-np:NP842836.RAaDiicIsbaIdbttp0LOy6oy57tmRKWZyyAghZqChWMSg130_assertion dcterms:description
      "[A recent genome-wide association study (GWAS) showed that two new susceptibility loci between EDIL3 and HAPLN1 at 5q14.3 (rs4552569) and within ANO6 at 12q12 (rs17095830) contribute to the risk of AS in Han Chinese.]. 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:23308121;
    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:NP842836.RAaDiicIsbaIdbttp0LOy6oy57tmRKWZyyAghZqChWMSg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:35+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" .
}