@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP178575.RAhZTiVOOkr9ip2ChinErGI4BELtBtvqh7vQqGb2qd2gk> .
@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:NP178575.RAhZTiVOOkr9ip2ChinErGI4BELtBtvqh7vQqGb2qd2gk130_head {
  this: np:hasAssertion dgn-np:NP178575.RAhZTiVOOkr9ip2ChinErGI4BELtBtvqh7vQqGb2qd2gk130_assertion ;
    np:hasProvenance dgn-np:NP178575.RAhZTiVOOkr9ip2ChinErGI4BELtBtvqh7vQqGb2qd2gk130_provenance ;
    np:hasPublicationInfo dgn-np:NP178575.RAhZTiVOOkr9ip2ChinErGI4BELtBtvqh7vQqGb2qd2gk130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP178575.RAhZTiVOOkr9ip2ChinErGI4BELtBtvqh7vQqGb2qd2gk130_assertion a np:Assertion .
  dgn-np:NP178575.RAhZTiVOOkr9ip2ChinErGI4BELtBtvqh7vQqGb2qd2gk130_provenance a np:Provenance .
  dgn-np:NP178575.RAhZTiVOOkr9ip2ChinErGI4BELtBtvqh7vQqGb2qd2gk130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP178575.RAhZTiVOOkr9ip2ChinErGI4BELtBtvqh7vQqGb2qd2gk130_assertion {
  miriam-gene:407977 a ncit:C16612 .
  lld:C0917798 a ncit:C7057 .
  dgn-gda:DGN22a77d9fc651d5fbf1fbe8cf8eefd4fc sio:SIO_000628 miriam-gene:407977 , lld:C0917798 ;
    a sio:SIO_001121 .
}
dgn-np:NP178575.RAhZTiVOOkr9ip2ChinErGI4BELtBtvqh7vQqGb2qd2gk130_provenance {
  dgn-np:NP178575.RAhZTiVOOkr9ip2ChinErGI4BELtBtvqh7vQqGb2qd2gk130_assertion dcterms:description "[Recent studies have indicated that TWEAK and Fn14 are expressed in the central nervous system (CNS), and that in response to a variety of stimuli, including cerebral ischemia, there is an increase in TWEAK and Fn14 expression in perivascular astrocytes, microglia, endothelial cells, and neurons with subsequent increase in the permeability of the blood-brain barrier (BBB) and cell death.]. 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:17917114 ;
    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:NP178575.RAhZTiVOOkr9ip2ChinErGI4BELtBtvqh7vQqGb2qd2gk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:36+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" .
}