@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP89585.RA9DNnFFPe70keMjRm5-cONjH4J0QZOrTjYLMpetVVJYg> .
@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:NP89585.RA9DNnFFPe70keMjRm5-cONjH4J0QZOrTjYLMpetVVJYg130_head {
  this: np:hasAssertion dgn-np:NP89585.RA9DNnFFPe70keMjRm5-cONjH4J0QZOrTjYLMpetVVJYg130_assertion;
    np:hasProvenance dgn-np:NP89585.RA9DNnFFPe70keMjRm5-cONjH4J0QZOrTjYLMpetVVJYg130_provenance;
    np:hasPublicationInfo dgn-np:NP89585.RA9DNnFFPe70keMjRm5-cONjH4J0QZOrTjYLMpetVVJYg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP89585.RA9DNnFFPe70keMjRm5-cONjH4J0QZOrTjYLMpetVVJYg130_assertion a np:Assertion .
  
  dgn-np:NP89585.RA9DNnFFPe70keMjRm5-cONjH4J0QZOrTjYLMpetVVJYg130_provenance a np:Provenance .
  
  dgn-np:NP89585.RA9DNnFFPe70keMjRm5-cONjH4J0QZOrTjYLMpetVVJYg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP89585.RA9DNnFFPe70keMjRm5-cONjH4J0QZOrTjYLMpetVVJYg130_assertion {
  miriam-gene:121278 a ncit:C16612 .
  
  lld:C0033931 a ncit:C7057 .
  
  dgn-gda:DGN467b02edf912c95d9bbf0f94de3f1950 sio:SIO_000628 miriam-gene:121278, lld:C0033931;
    a sio:SIO_001122 .
}

dgn-np:NP89585.RA9DNnFFPe70keMjRm5-cONjH4J0QZOrTjYLMpetVVJYg130_provenance {
  dgn-np:NP89585.RA9DNnFFPe70keMjRm5-cONjH4J0QZOrTjYLMpetVVJYg130_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:NP89585.RA9DNnFFPe70keMjRm5-cONjH4J0QZOrTjYLMpetVVJYg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:44+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>,
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
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