@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP258925.RAemTTdcyKPC7np8yO1niTdli-bmxjJ3epdjT2xRcEMLA> .
@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:NP258925.RAemTTdcyKPC7np8yO1niTdli-bmxjJ3epdjT2xRcEMLA130_head {
  this: np:hasAssertion dgn-np:NP258925.RAemTTdcyKPC7np8yO1niTdli-bmxjJ3epdjT2xRcEMLA130_assertion;
    np:hasProvenance dgn-np:NP258925.RAemTTdcyKPC7np8yO1niTdli-bmxjJ3epdjT2xRcEMLA130_provenance;
    np:hasPublicationInfo dgn-np:NP258925.RAemTTdcyKPC7np8yO1niTdli-bmxjJ3epdjT2xRcEMLA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP258925.RAemTTdcyKPC7np8yO1niTdli-bmxjJ3epdjT2xRcEMLA130_assertion a np:Assertion .
  
  dgn-np:NP258925.RAemTTdcyKPC7np8yO1niTdli-bmxjJ3epdjT2xRcEMLA130_provenance a np:Provenance .
  
  dgn-np:NP258925.RAemTTdcyKPC7np8yO1niTdli-bmxjJ3epdjT2xRcEMLA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP258925.RAemTTdcyKPC7np8yO1niTdli-bmxjJ3epdjT2xRcEMLA130_assertion {
  miriam-gene:1312 a ncit:C16612 .
  
  lld:C0004936 a ncit:C7057 .
  
  dgn-gda:DGN82ad4dc076a9d3080da90d1e5346e0ae sio:SIO_000628 miriam-gene:1312, lld:C0004936;
    a sio:SIO_001121 .
}

dgn-np:NP258925.RAemTTdcyKPC7np8yO1niTdli-bmxjJ3epdjT2xRcEMLA130_provenance {
  dgn-np:NP258925.RAemTTdcyKPC7np8yO1niTdli-bmxjJ3epdjT2xRcEMLA130_assertion dcterms:description
      "[Future longitudinal studies focusing on additional COMT polymorphic sites and other candidate genes from the deleted region will elucidate the molecular pathways leading to schizophrenia and other psychiatric disorders in VCFS.]. 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:16734939;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  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;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}

dgn-np:NP258925.RAemTTdcyKPC7np8yO1niTdli-bmxjJ3epdjT2xRcEMLA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:24+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" .
}