@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP9969.RA4_sx56Ac5bEVA7LV9H3nOXpoyEmjWT3NJQm1TqU2aZ8> .
@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:NP9969.RA4_sx56Ac5bEVA7LV9H3nOXpoyEmjWT3NJQm1TqU2aZ8130_head {
  this: np:hasAssertion dgn-np:NP9969.RA4_sx56Ac5bEVA7LV9H3nOXpoyEmjWT3NJQm1TqU2aZ8130_assertion;
    np:hasProvenance dgn-np:NP9969.RA4_sx56Ac5bEVA7LV9H3nOXpoyEmjWT3NJQm1TqU2aZ8130_provenance;
    np:hasPublicationInfo dgn-np:NP9969.RA4_sx56Ac5bEVA7LV9H3nOXpoyEmjWT3NJQm1TqU2aZ8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP9969.RA4_sx56Ac5bEVA7LV9H3nOXpoyEmjWT3NJQm1TqU2aZ8130_assertion a np:Assertion .
  
  dgn-np:NP9969.RA4_sx56Ac5bEVA7LV9H3nOXpoyEmjWT3NJQm1TqU2aZ8130_provenance a np:Provenance .
  
  dgn-np:NP9969.RA4_sx56Ac5bEVA7LV9H3nOXpoyEmjWT3NJQm1TqU2aZ8130_publicationInfo a np:PublicationInfo .
}

dgn-np:NP9969.RA4_sx56Ac5bEVA7LV9H3nOXpoyEmjWT3NJQm1TqU2aZ8130_assertion {
  miriam-gene:627 a ncit:C16612 .
  
  lld:C0038220 a ncit:C7057 .
  
  dgn-gda:DGN012f12fa94c215d0f061f57fee9a071b sio:SIO_000628 miriam-gene:627, lld:C0038220;
    a sio:SIO_001121 .
}

dgn-np:NP9969.RA4_sx56Ac5bEVA7LV9H3nOXpoyEmjWT3NJQm1TqU2aZ8130_provenance {
  dgn-np:NP9969.RA4_sx56Ac5bEVA7LV9H3nOXpoyEmjWT3NJQm1TqU2aZ8130_assertion dcterms:description
      "[These results provide a complete description of changes in mRNA levels of neurotrophins and their receptors in the forebrain after SE and supply additional data supporting the view that neurotrophin gene expression is related to abnormal neuronal activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_curated;
    sio:SIO_000772 miriam-pubmed:8635431;
    prov:wasDerivedFrom dgn-void:ctd_human-20130708;
    prov:wasGeneratedBy eco:ECO_0000218 .
  
  dgn-void:ctd_human-20130708 pav:importedOn "2013-07-24"^^xsd:date .
  
  dgn-void:source_evidence_curated a eco:ECO_0000205;
    rdfs:comment "Gene-disease associations manually curated."@en;
    rdfs:label "DisGeNET evidence - CURATED"@en .
}

dgn-np:NP9969.RA4_sx56Ac5bEVA7LV9H3nOXpoyEmjWT3NJQm1TqU2aZ8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:02+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" .
}