@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP83751.RA822PdwJeV-O_nhBAt95ZY4x5u23Pafeg6nw447xabt8> .
@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 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:NP83751.RA822PdwJeV-O_nhBAt95ZY4x5u23Pafeg6nw447xabt8130_head {
  this: np:hasAssertion dgn-np:NP83751.RA822PdwJeV-O_nhBAt95ZY4x5u23Pafeg6nw447xabt8130_assertion;
    np:hasProvenance dgn-np:NP83751.RA822PdwJeV-O_nhBAt95ZY4x5u23Pafeg6nw447xabt8130_provenance;
    np:hasPublicationInfo dgn-np:NP83751.RA822PdwJeV-O_nhBAt95ZY4x5u23Pafeg6nw447xabt8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP83751.RA822PdwJeV-O_nhBAt95ZY4x5u23Pafeg6nw447xabt8130_assertion a np:Assertion .
  
  dgn-np:NP83751.RA822PdwJeV-O_nhBAt95ZY4x5u23Pafeg6nw447xabt8130_provenance a np:Provenance .
  
  dgn-np:NP83751.RA822PdwJeV-O_nhBAt95ZY4x5u23Pafeg6nw447xabt8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP83751.RA822PdwJeV-O_nhBAt95ZY4x5u23Pafeg6nw447xabt8130_assertion {
  miriam-gene:2908 a ncit:C16612 .
  
  lld:C0033931 a ncit:C7057 .
  
  dgn-gda:DGN9e767bf51d6464a2dff913763b61d8ab sio:SIO_000628 miriam-gene:2908, lld:C0033931;
    a sio:SIO_001122 .
}

dgn-np:NP83751.RA822PdwJeV-O_nhBAt95ZY4x5u23Pafeg6nw447xabt8130_provenance {
  dgn-np:NP83751.RA822PdwJeV-O_nhBAt95ZY4x5u23Pafeg6nw447xabt8130_assertion dct:description
      "[This study finds association of SNPs in HTR2A, SERPINA6, and TPH2 with somatic symptoms implicating them as potentially important in the shared genetic component to functional somatic syndromes, although replication is required.]. 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:20403506;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP83751.RA822PdwJeV-O_nhBAt95ZY4x5u23Pafeg6nw447xabt8130_publicationInfo {
  this: dct:created "2014-10-02T12:32:41+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}