@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP669005.RAi9y1wf1rLd55KVeJ1U8q6DMXY8OukVaad3KxpJtNK_g> .
@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:NP669005.RAi9y1wf1rLd55KVeJ1U8q6DMXY8OukVaad3KxpJtNK_g130_head {
  this: np:hasAssertion dgn-np:NP669005.RAi9y1wf1rLd55KVeJ1U8q6DMXY8OukVaad3KxpJtNK_g130_assertion;
    np:hasProvenance dgn-np:NP669005.RAi9y1wf1rLd55KVeJ1U8q6DMXY8OukVaad3KxpJtNK_g130_provenance;
    np:hasPublicationInfo dgn-np:NP669005.RAi9y1wf1rLd55KVeJ1U8q6DMXY8OukVaad3KxpJtNK_g130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP669005.RAi9y1wf1rLd55KVeJ1U8q6DMXY8OukVaad3KxpJtNK_g130_assertion a np:Assertion .
  
  dgn-np:NP669005.RAi9y1wf1rLd55KVeJ1U8q6DMXY8OukVaad3KxpJtNK_g130_provenance a np:Provenance .
  
  dgn-np:NP669005.RAi9y1wf1rLd55KVeJ1U8q6DMXY8OukVaad3KxpJtNK_g130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP669005.RAi9y1wf1rLd55KVeJ1U8q6DMXY8OukVaad3KxpJtNK_g130_assertion {
  miriam-gene:2896 a ncit:C16612 .
  
  lld:C0005586 a ncit:C7057 .
  
  dgn-gda:DGN43259bc075a8167b93aeab21852c2d62 sio:SIO_000628 miriam-gene:2896, lld:C0005586;
    a sio:SIO_001121 .
}

dgn-np:NP669005.RAi9y1wf1rLd55KVeJ1U8q6DMXY8OukVaad3KxpJtNK_g130_provenance {
  dgn-np:NP669005.RAi9y1wf1rLd55KVeJ1U8q6DMXY8OukVaad3KxpJtNK_g130_assertion dcterms:description
      "[Basing on the assumption that frontotemporal lobar degeneration (FTLD), schizophrenia and bipolar disorder (BPD) might share common aetiological mechanisms, we analyzed genetic variation in the FTLD risk gene progranulin (GRN) in a German population of patients with schizophrenia (n = 271) or BPD (n = 237) as compared with 574 age-, gender- and ethnicity-matched controls.]. 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:22505994;
    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:NP669005.RAi9y1wf1rLd55KVeJ1U8q6DMXY8OukVaad3KxpJtNK_g130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:44+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" .
}