@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP136909.RAPMeqL7ysCvK1Bi_N8E8OothpY10KUQeQotoVBSwg_hc> .
@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/v3.0.0/void/> .

dgn-np:NP136909.RAPMeqL7ysCvK1Bi_N8E8OothpY10KUQeQotoVBSwg_hc130_head {
  this: np:hasAssertion dgn-np:NP136909.RAPMeqL7ysCvK1Bi_N8E8OothpY10KUQeQotoVBSwg_hc130_assertion;
    np:hasProvenance dgn-np:NP136909.RAPMeqL7ysCvK1Bi_N8E8OothpY10KUQeQotoVBSwg_hc130_provenance;
    np:hasPublicationInfo dgn-np:NP136909.RAPMeqL7ysCvK1Bi_N8E8OothpY10KUQeQotoVBSwg_hc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP136909.RAPMeqL7ysCvK1Bi_N8E8OothpY10KUQeQotoVBSwg_hc130_assertion a np:Assertion .
  
  dgn-np:NP136909.RAPMeqL7ysCvK1Bi_N8E8OothpY10KUQeQotoVBSwg_hc130_provenance a np:Provenance .
  
  dgn-np:NP136909.RAPMeqL7ysCvK1Bi_N8E8OothpY10KUQeQotoVBSwg_hc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP136909.RAPMeqL7ysCvK1Bi_N8E8OothpY10KUQeQotoVBSwg_hc130_assertion {
  miriam-gene:3357 a ncit:C16612 .
  
  lld:C0015672 a ncit:C7057 .
  
  dgn-gda:DGN8a3eba3874ef0cde9712e6515bfcdfe0 sio:SIO_000628 miriam-gene:3357, lld:C0015672;
    a sio:SIO_001122 .
}

dgn-np:NP136909.RAPMeqL7ysCvK1Bi_N8E8OothpY10KUQeQotoVBSwg_hc130_provenance {
  dgn-np:NP136909.RAPMeqL7ysCvK1Bi_N8E8OothpY10KUQeQotoVBSwg_hc130_assertion dcterms:description
      "[A total of 77 polymorphisms in genes related to serotonin synthesis (TPH2), signaling (HTR1A, HTR1E, HTR2A, HTR2B, HTR2C, HTR3A, HTR3B, HTR4, HTR5A, HTR6, and HTR7), transport (SLC6A4), and catabolism (MAOA) were examined in 137 clinically evaluated subjects (40 CFS, 55 with insufficient fatigue, and 42 non-fatigued, NF, controls) derived from a population-based CFS surveillance study in Wichita, Kansas.]. 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:18079067;
    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:NP136909.RAPMeqL7ysCvK1Bi_N8E8OothpY10KUQeQotoVBSwg_hc130_publicationInfo {
  this: dcterms:created "2015-08-25T14:38:57+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}