@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP179951.RANIu0dds68tmeUTPbCcr1MLeKYgdGacf3KkeXJCj0AUc> .
@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:NP179951.RANIu0dds68tmeUTPbCcr1MLeKYgdGacf3KkeXJCj0AUc130_head {
  this: np:hasAssertion dgn-np:NP179951.RANIu0dds68tmeUTPbCcr1MLeKYgdGacf3KkeXJCj0AUc130_assertion;
    np:hasProvenance dgn-np:NP179951.RANIu0dds68tmeUTPbCcr1MLeKYgdGacf3KkeXJCj0AUc130_provenance;
    np:hasPublicationInfo dgn-np:NP179951.RANIu0dds68tmeUTPbCcr1MLeKYgdGacf3KkeXJCj0AUc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP179951.RANIu0dds68tmeUTPbCcr1MLeKYgdGacf3KkeXJCj0AUc130_assertion a np:Assertion .
  
  dgn-np:NP179951.RANIu0dds68tmeUTPbCcr1MLeKYgdGacf3KkeXJCj0AUc130_provenance a np:Provenance .
  
  dgn-np:NP179951.RANIu0dds68tmeUTPbCcr1MLeKYgdGacf3KkeXJCj0AUc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP179951.RANIu0dds68tmeUTPbCcr1MLeKYgdGacf3KkeXJCj0AUc130_assertion {
  miriam-gene:57030 a ncit:C16612 .
  
  lld:C0595905 a ncit:C7057 .
  
  dgn-gda:DGN2b65b447d9402d1b011c9783f7b31172 sio:SIO_000628 miriam-gene:57030, lld:C0595905;
    a sio:SIO_001121 .
}

dgn-np:NP179951.RANIu0dds68tmeUTPbCcr1MLeKYgdGacf3KkeXJCj0AUc130_provenance {
  dgn-np:NP179951.RANIu0dds68tmeUTPbCcr1MLeKYgdGacf3KkeXJCj0AUc130_assertion dcterms:description
      "[In the hippocampus, the loss of VGLUT1 mRNA supports data indicating that glutamatergic presynaptic deficits are prominent, whereas the pattern of results in temporal and frontal cortex suggests broadly similar changes may affect inhibitory and excitatory neurons.]. 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:15653259;
    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:NP179951.RANIu0dds68tmeUTPbCcr1MLeKYgdGacf3KkeXJCj0AUc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:37+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" .
}