@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP86472.RA2AxS8ydcl1Zt5wuNChsG84S9y1LXMTPC5VOyudazGVY> .
@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:NP86472.RA2AxS8ydcl1Zt5wuNChsG84S9y1LXMTPC5VOyudazGVY130_head {
  this: np:hasAssertion dgn-np:NP86472.RA2AxS8ydcl1Zt5wuNChsG84S9y1LXMTPC5VOyudazGVY130_assertion;
    np:hasProvenance dgn-np:NP86472.RA2AxS8ydcl1Zt5wuNChsG84S9y1LXMTPC5VOyudazGVY130_provenance;
    np:hasPublicationInfo dgn-np:NP86472.RA2AxS8ydcl1Zt5wuNChsG84S9y1LXMTPC5VOyudazGVY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP86472.RA2AxS8ydcl1Zt5wuNChsG84S9y1LXMTPC5VOyudazGVY130_assertion a np:Assertion .
  
  dgn-np:NP86472.RA2AxS8ydcl1Zt5wuNChsG84S9y1LXMTPC5VOyudazGVY130_provenance a np:Provenance .
  
  dgn-np:NP86472.RA2AxS8ydcl1Zt5wuNChsG84S9y1LXMTPC5VOyudazGVY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP86472.RA2AxS8ydcl1Zt5wuNChsG84S9y1LXMTPC5VOyudazGVY130_assertion {
  miriam-gene:3356 a ncit:C16612 .
  
  lld:C0033931 a ncit:C7057 .
  
  dgn-gda:DGN045627e67ead649b786c9ac175b3acab sio:SIO_000628 miriam-gene:3356, lld:C0033931;
    a sio:SIO_001122 .
}

dgn-np:NP86472.RA2AxS8ydcl1Zt5wuNChsG84S9y1LXMTPC5VOyudazGVY130_provenance {
  dgn-np:NP86472.RA2AxS8ydcl1Zt5wuNChsG84S9y1LXMTPC5VOyudazGVY130_assertion dcterms: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:NP86472.RA2AxS8ydcl1Zt5wuNChsG84S9y1LXMTPC5VOyudazGVY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:42+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" .
}