@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP265727.RAe5gRtjvDNrYIQFLlDrMcSNYFXd8cNdaoEoWhCgr-yiU> .
@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:NP265727.RAe5gRtjvDNrYIQFLlDrMcSNYFXd8cNdaoEoWhCgr-yiU130_head {
  this: np:hasAssertion dgn-np:NP265727.RAe5gRtjvDNrYIQFLlDrMcSNYFXd8cNdaoEoWhCgr-yiU130_assertion;
    np:hasProvenance dgn-np:NP265727.RAe5gRtjvDNrYIQFLlDrMcSNYFXd8cNdaoEoWhCgr-yiU130_provenance;
    np:hasPublicationInfo dgn-np:NP265727.RAe5gRtjvDNrYIQFLlDrMcSNYFXd8cNdaoEoWhCgr-yiU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP265727.RAe5gRtjvDNrYIQFLlDrMcSNYFXd8cNdaoEoWhCgr-yiU130_assertion a np:Assertion .
  
  dgn-np:NP265727.RAe5gRtjvDNrYIQFLlDrMcSNYFXd8cNdaoEoWhCgr-yiU130_provenance a np:Provenance .
  
  dgn-np:NP265727.RAe5gRtjvDNrYIQFLlDrMcSNYFXd8cNdaoEoWhCgr-yiU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP265727.RAe5gRtjvDNrYIQFLlDrMcSNYFXd8cNdaoEoWhCgr-yiU130_assertion {
  miriam-gene:1312 a ncit:C16612 .
  
  lld:C0003469 a ncit:C7057 .
  
  dgn-gda:DGN4fa17768c28a61a51852f8a742cf9d1d sio:SIO_000628 miriam-gene:1312, lld:C0003469;
    a sio:SIO_001121 .
}

dgn-np:NP265727.RAe5gRtjvDNrYIQFLlDrMcSNYFXd8cNdaoEoWhCgr-yiU130_provenance {
  dgn-np:NP265727.RAe5gRtjvDNrYIQFLlDrMcSNYFXd8cNdaoEoWhCgr-yiU130_assertion dcterms:description
      "[Since pain syndromes as well as anxiety and depression are associated to low and high COMT activity respectively and these conditions are all associated with irritable bowel syndrome (IBS) we wanted for the first time to explore the relationship between the polymorphism and IBS.]. 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:21437260;
    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:NP265727.RAe5gRtjvDNrYIQFLlDrMcSNYFXd8cNdaoEoWhCgr-yiU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:28+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" .
}