@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP435693.RAKESllQPH5vK8SpmAoRpdxU3d9OWY_GeVm_Elv91erco> .
@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:NP435693.RAKESllQPH5vK8SpmAoRpdxU3d9OWY_GeVm_Elv91erco130_head {
  this: np:hasAssertion dgn-np:NP435693.RAKESllQPH5vK8SpmAoRpdxU3d9OWY_GeVm_Elv91erco130_assertion;
    np:hasProvenance dgn-np:NP435693.RAKESllQPH5vK8SpmAoRpdxU3d9OWY_GeVm_Elv91erco130_provenance;
    np:hasPublicationInfo dgn-np:NP435693.RAKESllQPH5vK8SpmAoRpdxU3d9OWY_GeVm_Elv91erco130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP435693.RAKESllQPH5vK8SpmAoRpdxU3d9OWY_GeVm_Elv91erco130_assertion a np:Assertion .
  
  dgn-np:NP435693.RAKESllQPH5vK8SpmAoRpdxU3d9OWY_GeVm_Elv91erco130_provenance a np:Provenance .
  
  dgn-np:NP435693.RAKESllQPH5vK8SpmAoRpdxU3d9OWY_GeVm_Elv91erco130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP435693.RAKESllQPH5vK8SpmAoRpdxU3d9OWY_GeVm_Elv91erco130_assertion {
  miriam-gene:1312 a ncit:C16612 .
  
  lld:C0016053 a ncit:C7057 .
  
  dgn-gda:DGN934109a8f42bca608c5b0f559a49b53f sio:SIO_000628 miriam-gene:1312, lld:C0016053;
    a sio:SIO_001121 .
}

dgn-np:NP435693.RAKESllQPH5vK8SpmAoRpdxU3d9OWY_GeVm_Elv91erco130_provenance {
  dgn-np:NP435693.RAKESllQPH5vK8SpmAoRpdxU3d9OWY_GeVm_Elv91erco130_assertion dcterms:description
      "[In conclusion, COMT polymorphism is of potential pharmacological importance regarding individual differences in the metabolism of catechol drugs and may also be involved in the pathogenesis and treatment of FS through adrenergic mechanisms as well as genetic predisposition to FS.]. 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:12739038;
    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:NP435693.RAKESllQPH5vK8SpmAoRpdxU3d9OWY_GeVm_Elv91erco130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:18+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" .
}