@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP55024.RA2saFndTGKnRkNbLDD5uy5iR3tJR0MPBX7DDt05nOhxg> .
@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:NP55024.RA2saFndTGKnRkNbLDD5uy5iR3tJR0MPBX7DDt05nOhxg130_head {
  this: np:hasAssertion dgn-np:NP55024.RA2saFndTGKnRkNbLDD5uy5iR3tJR0MPBX7DDt05nOhxg130_assertion;
    np:hasProvenance dgn-np:NP55024.RA2saFndTGKnRkNbLDD5uy5iR3tJR0MPBX7DDt05nOhxg130_provenance;
    np:hasPublicationInfo dgn-np:NP55024.RA2saFndTGKnRkNbLDD5uy5iR3tJR0MPBX7DDt05nOhxg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP55024.RA2saFndTGKnRkNbLDD5uy5iR3tJR0MPBX7DDt05nOhxg130_assertion a np:Assertion .
  
  dgn-np:NP55024.RA2saFndTGKnRkNbLDD5uy5iR3tJR0MPBX7DDt05nOhxg130_provenance a np:Provenance .
  
  dgn-np:NP55024.RA2saFndTGKnRkNbLDD5uy5iR3tJR0MPBX7DDt05nOhxg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP55024.RA2saFndTGKnRkNbLDD5uy5iR3tJR0MPBX7DDt05nOhxg130_assertion {
  miriam-gene:4128 a ncit:C16612 .
  
  lld:C0004352 a ncit:C7057 .
  
  dgn-gda:DGNd74815761369502c1de67a313482f84c sio:SIO_000628 miriam-gene:4128, lld:C0004352;
    a sio:SIO_001122 .
}

dgn-np:NP55024.RA2saFndTGKnRkNbLDD5uy5iR3tJR0MPBX7DDt05nOhxg130_provenance {
  dgn-np:NP55024.RA2saFndTGKnRkNbLDD5uy5iR3tJR0MPBX7DDt05nOhxg130_assertion dcterms:description
      "[Suggested mechanisms for hyperserotonemia in autism have been increased synthesis of serotonin (5HT) by tryptophan hydroxylase (TPH), increased uptake into platelets through 5HT transporter (5HTt), diminished release from platelets through 5HT2A receptor (5HT2Ar) and decreased metabolism by monoamine oxydase (MAOA).]. 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:18405062;
    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:NP55024.RA2saFndTGKnRkNbLDD5uy5iR3tJR0MPBX7DDt05nOhxg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:25+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" .
}