@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP711902.RAkRH2GilIFrpqxB0qVivb-gss5kF-H2LNLL7G4k-4b0E> .
@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:NP711902.RAkRH2GilIFrpqxB0qVivb-gss5kF-H2LNLL7G4k-4b0E130_head {
  this: np:hasAssertion dgn-np:NP711902.RAkRH2GilIFrpqxB0qVivb-gss5kF-H2LNLL7G4k-4b0E130_assertion;
    np:hasProvenance dgn-np:NP711902.RAkRH2GilIFrpqxB0qVivb-gss5kF-H2LNLL7G4k-4b0E130_provenance;
    np:hasPublicationInfo dgn-np:NP711902.RAkRH2GilIFrpqxB0qVivb-gss5kF-H2LNLL7G4k-4b0E130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP711902.RAkRH2GilIFrpqxB0qVivb-gss5kF-H2LNLL7G4k-4b0E130_assertion a np:Assertion .
  
  dgn-np:NP711902.RAkRH2GilIFrpqxB0qVivb-gss5kF-H2LNLL7G4k-4b0E130_provenance a np:Provenance .
  
  dgn-np:NP711902.RAkRH2GilIFrpqxB0qVivb-gss5kF-H2LNLL7G4k-4b0E130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP711902.RAkRH2GilIFrpqxB0qVivb-gss5kF-H2LNLL7G4k-4b0E130_assertion {
  miriam-gene:121278 a ncit:C16612 .
  
  lld:C0015672 a ncit:C7057 .
  
  dgn-gda:DGN22e0e2a5c76b274fc833fa2ded09992b sio:SIO_000628 miriam-gene:121278, lld:C0015672;
    a sio:SIO_001121 .
}

dgn-np:NP711902.RAkRH2GilIFrpqxB0qVivb-gss5kF-H2LNLL7G4k-4b0E130_provenance {
  dgn-np:NP711902.RAkRH2GilIFrpqxB0qVivb-gss5kF-H2LNLL7G4k-4b0E130_assertion dcterms:description
      "[Of the five classes of subjects with unexplained fatigue, three classes were distinguished by gene polymorphsims involved in either HPA axis function or neurotransmitter systems, including proopiomelanocortin (POMC), nuclear receptor subfamily 3, group C, member 1 (NR3C1), monoamine oxidase A (MAOA), monoamine oxidase B (MAOB), and tryptophan hydroxylase 2 (TPH2).]. 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:16610949;
    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:NP711902.RAkRH2GilIFrpqxB0qVivb-gss5kF-H2LNLL7G4k-4b0E130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:12+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" .
}