@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP397215.RAbp_sio6HgqpIGS44n9xes0DISxONnruep7gc8z2-G80> .
@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:NP397215.RAbp_sio6HgqpIGS44n9xes0DISxONnruep7gc8z2-G80130_head {
  this: np:hasAssertion dgn-np:NP397215.RAbp_sio6HgqpIGS44n9xes0DISxONnruep7gc8z2-G80130_assertion ;
    np:hasProvenance dgn-np:NP397215.RAbp_sio6HgqpIGS44n9xes0DISxONnruep7gc8z2-G80130_provenance ;
    np:hasPublicationInfo dgn-np:NP397215.RAbp_sio6HgqpIGS44n9xes0DISxONnruep7gc8z2-G80130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP397215.RAbp_sio6HgqpIGS44n9xes0DISxONnruep7gc8z2-G80130_assertion a np:Assertion .
  dgn-np:NP397215.RAbp_sio6HgqpIGS44n9xes0DISxONnruep7gc8z2-G80130_provenance a np:Provenance .
  dgn-np:NP397215.RAbp_sio6HgqpIGS44n9xes0DISxONnruep7gc8z2-G80130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP397215.RAbp_sio6HgqpIGS44n9xes0DISxONnruep7gc8z2-G80130_assertion {
  miriam-gene:3106 a ncit:C16612 .
  lld:C0949691 a ncit:C7057 .
  dgn-gda:DGNc85a7284e540ded8c0b178ef1c2126fb sio:SIO_000628 miriam-gene:3106 , lld:C0949691 ;
    a sio:SIO_001121 .
}
dgn-np:NP397215.RAbp_sio6HgqpIGS44n9xes0DISxONnruep7gc8z2-G80130_provenance {
  dgn-np:NP397215.RAbp_sio6HgqpIGS44n9xes0DISxONnruep7gc8z2-G80130_assertion dcterms:description "[Moreover, in other forms of spondyloarthropathy, a similar association has been reported: 42% of patients with spondyloarthropathy and associated asymptomatic chronic gut inflammation, who are considered likely to develop Crohn's disease and ankylosing spondylitis, are carriers of at least one CARD15 mutation, compared with only 7% of patients with normal histology.]. 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:15352892 ;
    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:NP397215.RAbp_sio6HgqpIGS44n9xes0DISxONnruep7gc8z2-G80130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:56+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" .
}