@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP237028.RAgi2VttmkH1W0sfcD--RBZ7iAS9it1HBrUaqzINsqNac> .
@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:NP237028.RAgi2VttmkH1W0sfcD--RBZ7iAS9it1HBrUaqzINsqNac130_head {
  this: np:hasAssertion dgn-np:NP237028.RAgi2VttmkH1W0sfcD--RBZ7iAS9it1HBrUaqzINsqNac130_assertion;
    np:hasProvenance dgn-np:NP237028.RAgi2VttmkH1W0sfcD--RBZ7iAS9it1HBrUaqzINsqNac130_provenance;
    np:hasPublicationInfo dgn-np:NP237028.RAgi2VttmkH1W0sfcD--RBZ7iAS9it1HBrUaqzINsqNac130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP237028.RAgi2VttmkH1W0sfcD--RBZ7iAS9it1HBrUaqzINsqNac130_assertion a np:Assertion .
  
  dgn-np:NP237028.RAgi2VttmkH1W0sfcD--RBZ7iAS9it1HBrUaqzINsqNac130_provenance a np:Provenance .
  
  dgn-np:NP237028.RAgi2VttmkH1W0sfcD--RBZ7iAS9it1HBrUaqzINsqNac130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP237028.RAgi2VttmkH1W0sfcD--RBZ7iAS9it1HBrUaqzINsqNac130_assertion {
  miriam-gene:6583 a ncit:C16612 .
  
  lld:C0009324 a ncit:C7057 .
  
  dgn-gda:DGNb5556f7f02154775a966a7212a078119 sio:SIO_000628 miriam-gene:6583, lld:C0009324;
    a sio:SIO_001121 .
}

dgn-np:NP237028.RAgi2VttmkH1W0sfcD--RBZ7iAS9it1HBrUaqzINsqNac130_provenance {
  dgn-np:NP237028.RAgi2VttmkH1W0sfcD--RBZ7iAS9it1HBrUaqzINsqNac130_assertion dcterms:description
      "[The aim of this study was to verify the prevalence rate of the haplotype called TC, determined by combination of two functional alleles of OCTN cation transporter genes (SLC22A4 1672T and SLC22A5 -207C combination variants) in ulcerative colitis patients and unrelated 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:17387389;
    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:NP237028.RAgi2VttmkH1W0sfcD--RBZ7iAS9it1HBrUaqzINsqNac130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:13+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" .
}