@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP720149.RA5PI4UX33F8vclNrDHZQCX06hBGLvKdvJ2QCVSiCo3LU> .
@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:NP720149.RA5PI4UX33F8vclNrDHZQCX06hBGLvKdvJ2QCVSiCo3LU130_head {
  this: np:hasAssertion dgn-np:NP720149.RA5PI4UX33F8vclNrDHZQCX06hBGLvKdvJ2QCVSiCo3LU130_assertion;
    np:hasProvenance dgn-np:NP720149.RA5PI4UX33F8vclNrDHZQCX06hBGLvKdvJ2QCVSiCo3LU130_provenance;
    np:hasPublicationInfo dgn-np:NP720149.RA5PI4UX33F8vclNrDHZQCX06hBGLvKdvJ2QCVSiCo3LU130_publicationInfo;
    a np:Nanopublication .
  
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      np:PublicationInfo .
}

dgn-np:NP720149.RA5PI4UX33F8vclNrDHZQCX06hBGLvKdvJ2QCVSiCo3LU130_assertion {
  miriam-gene:121278 a ncit:C16612 .
  
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dgn-np:NP720149.RA5PI4UX33F8vclNrDHZQCX06hBGLvKdvJ2QCVSiCo3LU130_provenance {
  dgn-np:NP720149.RA5PI4UX33F8vclNrDHZQCX06hBGLvKdvJ2QCVSiCo3LU130_assertion dcterms:description
      "[The propensity of TPH2 to misfold upon oxidation of its cysteine residues is responsible for its catalytic lability and may be related to loss of serotonin neuronal function in PD and the emergence of non-motor (psychiatric) symptoms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
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  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;
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dgn-np:NP720149.RA5PI4UX33F8vclNrDHZQCX06hBGLvKdvJ2QCVSiCo3LU130_publicationInfo {
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    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dcterms:rightsHolder dgn-void:IBIGroup;
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    prv:usedData dgn-void:disgenetrdf;
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