@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP136993.RAuTi4hv9zi2U0ioE2F4xORII27fsTkymOYU5xm706DfU> .
@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:NP136993.RAuTi4hv9zi2U0ioE2F4xORII27fsTkymOYU5xm706DfU130_head {
  this: np:hasAssertion dgn-np:NP136993.RAuTi4hv9zi2U0ioE2F4xORII27fsTkymOYU5xm706DfU130_assertion;
    np:hasProvenance dgn-np:NP136993.RAuTi4hv9zi2U0ioE2F4xORII27fsTkymOYU5xm706DfU130_provenance;
    np:hasPublicationInfo dgn-np:NP136993.RAuTi4hv9zi2U0ioE2F4xORII27fsTkymOYU5xm706DfU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP136993.RAuTi4hv9zi2U0ioE2F4xORII27fsTkymOYU5xm706DfU130_assertion a np:Assertion .
  
  dgn-np:NP136993.RAuTi4hv9zi2U0ioE2F4xORII27fsTkymOYU5xm706DfU130_provenance a np:Provenance .
  
  dgn-np:NP136993.RAuTi4hv9zi2U0ioE2F4xORII27fsTkymOYU5xm706DfU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP136993.RAuTi4hv9zi2U0ioE2F4xORII27fsTkymOYU5xm706DfU130_assertion {
  miriam-gene:1312 a ncit:C16612 .
  
  lld:C0030193 a ncit:C7057 .
  
  dgn-gda:DGNf6e4cd8eec1905cba205e0925c9667b0 sio:SIO_000628 miriam-gene:1312, lld:C0030193;
    a sio:SIO_001122 .
}

dgn-np:NP136993.RAuTi4hv9zi2U0ioE2F4xORII27fsTkymOYU5xm706DfU130_provenance {
  dgn-np:NP136993.RAuTi4hv9zi2U0ioE2F4xORII27fsTkymOYU5xm706DfU130_assertion dcterms:description
      "[This study suggests that genetic variability in the COMT gene influence the efficacy of morphine in cancer patients with pain, and that increased understanding of this variability is reached by expanding from analyses of single SNPs to haplotype construct]. 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:19094200;
    prov:wasDerivedFrom dgn-void:gad-20150221;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP136993.RAuTi4hv9zi2U0ioE2F4xORII27fsTkymOYU5xm706DfU130_publicationInfo {
  this: dcterms:created "2016-05-13T12:42:49+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" .
}