@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP176963.RAupWZXXaydrD_Kv31aWWVxseIfMi2Jtnl9SZux3BJids> .
@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:NP176963.RAupWZXXaydrD_Kv31aWWVxseIfMi2Jtnl9SZux3BJids130_head {
  this: np:hasAssertion dgn-np:NP176963.RAupWZXXaydrD_Kv31aWWVxseIfMi2Jtnl9SZux3BJids130_assertion;
    np:hasProvenance dgn-np:NP176963.RAupWZXXaydrD_Kv31aWWVxseIfMi2Jtnl9SZux3BJids130_provenance;
    np:hasPublicationInfo dgn-np:NP176963.RAupWZXXaydrD_Kv31aWWVxseIfMi2Jtnl9SZux3BJids130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP176963.RAupWZXXaydrD_Kv31aWWVxseIfMi2Jtnl9SZux3BJids130_assertion a np:Assertion .
  
  dgn-np:NP176963.RAupWZXXaydrD_Kv31aWWVxseIfMi2Jtnl9SZux3BJids130_provenance a np:Provenance .
  
  dgn-np:NP176963.RAupWZXXaydrD_Kv31aWWVxseIfMi2Jtnl9SZux3BJids130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP176963.RAupWZXXaydrD_Kv31aWWVxseIfMi2Jtnl9SZux3BJids130_assertion {
  miriam-gene:7132 a ncit:C16612 .
  
  lld:C0038013 a ncit:C7057 .
  
  dgn-gda:DGNada02bd4e0a1d16d16e9df9ac7ecf433 sio:SIO_000628 miriam-gene:7132, lld:C0038013;
    a sio:SIO_001121 .
}

dgn-np:NP176963.RAupWZXXaydrD_Kv31aWWVxseIfMi2Jtnl9SZux3BJids130_provenance {
  dgn-np:NP176963.RAupWZXXaydrD_Kv31aWWVxseIfMi2Jtnl9SZux3BJids130_assertion dcterms:description
      "[In view of the previously reported associations of TNFRSF1A with AS, in Caucasians and Chinese, and the biological plausibility of this candidate gene, replication of this finding in well powered studies is clearly indicated.]. 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:22272576;
    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:NP176963.RAupWZXXaydrD_Kv31aWWVxseIfMi2Jtnl9SZux3BJids130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:35+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" .
}