@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP290837.RAqSnbl-Y1jXJcCYA841MzzVuuzlpzdIAe2x5T0pUZiyI> .
@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:NP290837.RAqSnbl-Y1jXJcCYA841MzzVuuzlpzdIAe2x5T0pUZiyI130_head {
  this: np:hasAssertion dgn-np:NP290837.RAqSnbl-Y1jXJcCYA841MzzVuuzlpzdIAe2x5T0pUZiyI130_assertion;
    np:hasProvenance dgn-np:NP290837.RAqSnbl-Y1jXJcCYA841MzzVuuzlpzdIAe2x5T0pUZiyI130_provenance;
    np:hasPublicationInfo dgn-np:NP290837.RAqSnbl-Y1jXJcCYA841MzzVuuzlpzdIAe2x5T0pUZiyI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP290837.RAqSnbl-Y1jXJcCYA841MzzVuuzlpzdIAe2x5T0pUZiyI130_assertion a np:Assertion .
  
  dgn-np:NP290837.RAqSnbl-Y1jXJcCYA841MzzVuuzlpzdIAe2x5T0pUZiyI130_provenance a np:Provenance .
  
  dgn-np:NP290837.RAqSnbl-Y1jXJcCYA841MzzVuuzlpzdIAe2x5T0pUZiyI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP290837.RAqSnbl-Y1jXJcCYA841MzzVuuzlpzdIAe2x5T0pUZiyI130_assertion {
  miriam-gene:5021 a ncit:C16612 .
  
  lld:C0022104 a ncit:C7057 .
  
  dgn-gda:DGNf65a11d194c118cc75bab866b046861d sio:SIO_000628 miriam-gene:5021, lld:C0022104;
    a sio:SIO_001121 .
}

dgn-np:NP290837.RAqSnbl-Y1jXJcCYA841MzzVuuzlpzdIAe2x5T0pUZiyI130_provenance {
  dgn-np:NP290837.RAqSnbl-Y1jXJcCYA841MzzVuuzlpzdIAe2x5T0pUZiyI130_assertion dcterms:description
      "[Genetic variants in the OXT promoter region, and in the OXTR gene in DNA samples from 131 rigorously evaluated patients with Irritable Bowel Syndrome (IBS), 408 homozygous subjects referred for lactase (LCT-13910 C>T, rs4988235) genotyping, and 299 asymptomatic blood donors were compared.]. 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:19943975;
    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:NP290837.RAqSnbl-Y1jXJcCYA841MzzVuuzlpzdIAe2x5T0pUZiyI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:45+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" .
}