@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP531011.RALTVVjsbzEz85Kq3OZpxFy6J6HqdGYXIK-2IjYyyGlm8> .
@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:NP531011.RALTVVjsbzEz85Kq3OZpxFy6J6HqdGYXIK-2IjYyyGlm8130_head {
  this: np:hasAssertion dgn-np:NP531011.RALTVVjsbzEz85Kq3OZpxFy6J6HqdGYXIK-2IjYyyGlm8130_assertion ;
    np:hasProvenance dgn-np:NP531011.RALTVVjsbzEz85Kq3OZpxFy6J6HqdGYXIK-2IjYyyGlm8130_provenance ;
    np:hasPublicationInfo dgn-np:NP531011.RALTVVjsbzEz85Kq3OZpxFy6J6HqdGYXIK-2IjYyyGlm8130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP531011.RALTVVjsbzEz85Kq3OZpxFy6J6HqdGYXIK-2IjYyyGlm8130_assertion a np:Assertion .
  dgn-np:NP531011.RALTVVjsbzEz85Kq3OZpxFy6J6HqdGYXIK-2IjYyyGlm8130_provenance a np:Provenance .
  dgn-np:NP531011.RALTVVjsbzEz85Kq3OZpxFy6J6HqdGYXIK-2IjYyyGlm8130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP531011.RALTVVjsbzEz85Kq3OZpxFy6J6HqdGYXIK-2IjYyyGlm8130_assertion {
  miriam-gene:3106 a ncit:C16612 .
  lld:C0949690 a ncit:C7057 .
  dgn-gda:DGNbe124199a33d7e715ca718b144d68938 sio:SIO_000628 miriam-gene:3106 , lld:C0949690 ;
    a sio:SIO_001121 .
}
dgn-np:NP531011.RALTVVjsbzEz85Kq3OZpxFy6J6HqdGYXIK-2IjYyyGlm8130_provenance {
  dgn-np:NP531011.RALTVVjsbzEz85Kq3OZpxFy6J6HqdGYXIK-2IjYyyGlm8130_assertion dcterms:description "[A case-control study of NOD2 polymorphisms known to be associated with Crohn's disease (CD) (Pro(268)Ser, Arg(702)Trp, Gly(908)Arg, and Leu(1007)fsinsC) was performed in 229 cases of primary AS with no diagnosed inflammatory bowel disease (IBD), 197 cases of AS associated with IBD (referred to as colitic spondylarthritis; comprising 78 with CD and 119 with ulcerative colitis [UC]), and 229 ethnically matched, healthy controls.]. 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:12115195 ;
    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:NP531011.RALTVVjsbzEz85Kq3OZpxFy6J6HqdGYXIK-2IjYyyGlm8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:21+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" .
}