@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP648976.RAumWse_nfE9OXUOetspUrx-PA4JX4dp86XHC2wC7-9HU> .
@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:NP648976.RAumWse_nfE9OXUOetspUrx-PA4JX4dp86XHC2wC7-9HU130_head {
  this: np:hasAssertion dgn-np:NP648976.RAumWse_nfE9OXUOetspUrx-PA4JX4dp86XHC2wC7-9HU130_assertion;
    np:hasProvenance dgn-np:NP648976.RAumWse_nfE9OXUOetspUrx-PA4JX4dp86XHC2wC7-9HU130_provenance;
    np:hasPublicationInfo dgn-np:NP648976.RAumWse_nfE9OXUOetspUrx-PA4JX4dp86XHC2wC7-9HU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP648976.RAumWse_nfE9OXUOetspUrx-PA4JX4dp86XHC2wC7-9HU130_assertion a np:Assertion .
  
  dgn-np:NP648976.RAumWse_nfE9OXUOetspUrx-PA4JX4dp86XHC2wC7-9HU130_provenance a np:Provenance .
  
  dgn-np:NP648976.RAumWse_nfE9OXUOetspUrx-PA4JX4dp86XHC2wC7-9HU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP648976.RAumWse_nfE9OXUOetspUrx-PA4JX4dp86XHC2wC7-9HU130_assertion {
  miriam-gene:4397 a ncit:C16612 .
  
  lld:C0030567 a ncit:C7057 .
  
  dgn-gda:DGNea18cb5201c7cb56c76a9a288f9a3fe4 sio:SIO_000628 miriam-gene:4397, lld:C0030567;
    a sio:SIO_001121 .
}

dgn-np:NP648976.RAumWse_nfE9OXUOetspUrx-PA4JX4dp86XHC2wC7-9HU130_provenance {
  dgn-np:NP648976.RAumWse_nfE9OXUOetspUrx-PA4JX4dp86XHC2wC7-9HU130_assertion dcterms:description
      "[Further, this laboratory is utilizing the optimized sensitive procedure to search for several virus etiologies in human diseases such as multiple sclerosis, temporal lobe epilepsy, Alzheimer's disease, schizophrenia, and Parkinson's disease, as well as normal aging.]. 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:3299127;
    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:NP648976.RAumWse_nfE9OXUOetspUrx-PA4JX4dp86XHC2wC7-9HU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:31+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" .
}