@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1080085.RAvohs9VgAz-FJjwcNVphXce_8tFGpDQX5loNRXDSFAk8> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP1080085.RAvohs9VgAz-FJjwcNVphXce_8tFGpDQX5loNRXDSFAk8130_head {
  this: np:hasAssertion dgn-np:NP1080085.RAvohs9VgAz-FJjwcNVphXce_8tFGpDQX5loNRXDSFAk8130_assertion;
    np:hasProvenance dgn-np:NP1080085.RAvohs9VgAz-FJjwcNVphXce_8tFGpDQX5loNRXDSFAk8130_provenance;
    np:hasPublicationInfo dgn-np:NP1080085.RAvohs9VgAz-FJjwcNVphXce_8tFGpDQX5loNRXDSFAk8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1080085.RAvohs9VgAz-FJjwcNVphXce_8tFGpDQX5loNRXDSFAk8130_assertion a np:Assertion .
  
  dgn-np:NP1080085.RAvohs9VgAz-FJjwcNVphXce_8tFGpDQX5loNRXDSFAk8130_provenance a np:Provenance .
  
  dgn-np:NP1080085.RAvohs9VgAz-FJjwcNVphXce_8tFGpDQX5loNRXDSFAk8130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1080085.RAvohs9VgAz-FJjwcNVphXce_8tFGpDQX5loNRXDSFAk8130_assertion {
  miriam-gene:1312 a ncit:C16612 .
  
  lld:C0030193 a ncit:C7057 .
  
  dgn-gda:DGNe1ed12b01fd326c1f2d29c7155834304 sio:SIO_000628 miriam-gene:1312, lld:C0030193;
    a sio:SIO_001121 .
}

dgn-np:NP1080085.RAvohs9VgAz-FJjwcNVphXce_8tFGpDQX5loNRXDSFAk8130_provenance {
  dgn-np:NP1080085.RAvohs9VgAz-FJjwcNVphXce_8tFGpDQX5loNRXDSFAk8130_assertion dcterms:description
      "[Both human and mouse COMT genes possess functional polymorphisms contributing to interindividual variability in pain phenotypes such as sensitivity to noxious stimuli, severity of clinical pain, and response to pain treatment.]. 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:23701723;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1080085.RAvohs9VgAz-FJjwcNVphXce_8tFGpDQX5loNRXDSFAk8130_publicationInfo {
  this: dcterms:created "2016-05-13T12:49:55+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}