@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP50379.RAQuWInwqEZuibOmAjF5OEO772sOxtcCHlfPQx74usTmk> .
@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:NP50379.RAQuWInwqEZuibOmAjF5OEO772sOxtcCHlfPQx74usTmk130_head {
  this: np:hasAssertion dgn-np:NP50379.RAQuWInwqEZuibOmAjF5OEO772sOxtcCHlfPQx74usTmk130_assertion;
    np:hasProvenance dgn-np:NP50379.RAQuWInwqEZuibOmAjF5OEO772sOxtcCHlfPQx74usTmk130_provenance;
    np:hasPublicationInfo dgn-np:NP50379.RAQuWInwqEZuibOmAjF5OEO772sOxtcCHlfPQx74usTmk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP50379.RAQuWInwqEZuibOmAjF5OEO772sOxtcCHlfPQx74usTmk130_assertion a np:Assertion .
  
  dgn-np:NP50379.RAQuWInwqEZuibOmAjF5OEO772sOxtcCHlfPQx74usTmk130_provenance a np:Provenance .
  
  dgn-np:NP50379.RAQuWInwqEZuibOmAjF5OEO772sOxtcCHlfPQx74usTmk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP50379.RAQuWInwqEZuibOmAjF5OEO772sOxtcCHlfPQx74usTmk130_assertion {
  miriam-gene:7099 a ncit:C16612 .
  
  lld:C0009324 a ncit:C7057 .
  
  dgn-gda:DGN5e0f48c4e956fa32cc90f89a4a23338c sio:SIO_000628 miriam-gene:7099, lld:C0009324;
    a sio:SIO_001122 .
}

dgn-np:NP50379.RAQuWInwqEZuibOmAjF5OEO772sOxtcCHlfPQx74usTmk130_provenance {
  dgn-np:NP50379.RAQuWInwqEZuibOmAjF5OEO772sOxtcCHlfPQx74usTmk130_assertion dcterms:description
      "[ CARD15 polymorphisms are seen in greater frequency in patients with pouchitis after IPAA for UC. These findings, if borne out in prospective analyses, suggest that CARD15 mutations, particularly L1007fsinsC, may predispose to the development of pouchitis after IPAA for UC.]. 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:16239841;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP50379.RAQuWInwqEZuibOmAjF5OEO772sOxtcCHlfPQx74usTmk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:23+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" .
}