@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP569195.RATREFQe9tLo0OItB9rZO3ytw2XZBatJ68NpFabjHU0Us> .
@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:NP569195.RATREFQe9tLo0OItB9rZO3ytw2XZBatJ68NpFabjHU0Us130_head {
  this: np:hasAssertion dgn-np:NP569195.RATREFQe9tLo0OItB9rZO3ytw2XZBatJ68NpFabjHU0Us130_assertion;
    np:hasProvenance dgn-np:NP569195.RATREFQe9tLo0OItB9rZO3ytw2XZBatJ68NpFabjHU0Us130_provenance;
    np:hasPublicationInfo dgn-np:NP569195.RATREFQe9tLo0OItB9rZO3ytw2XZBatJ68NpFabjHU0Us130_publicationInfo;
    a np:Nanopublication .
  
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  dgn-np:NP569195.RATREFQe9tLo0OItB9rZO3ytw2XZBatJ68NpFabjHU0Us130_publicationInfo a
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dgn-np:NP569195.RATREFQe9tLo0OItB9rZO3ytw2XZBatJ68NpFabjHU0Us130_assertion {
  miriam-gene:2896 a ncit:C16612 .
  
  lld:C0006012 a ncit:C7057 .
  
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    a sio:SIO_001121 .
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dgn-np:NP569195.RATREFQe9tLo0OItB9rZO3ytw2XZBatJ68NpFabjHU0Us130_provenance {
  dgn-np:NP569195.RATREFQe9tLo0OItB9rZO3ytw2XZBatJ68NpFabjHU0Us130_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;
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    prov:wasDerivedFrom dgn-void:befree-20140225;
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  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:NP569195.RATREFQe9tLo0OItB9rZO3ytw2XZBatJ68NpFabjHU0Us130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:43+02:00"^^xsd:dateTime;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dcterms:rightsHolder dgn-void:IBIGroup;
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    prv:usedData dgn-void:disgenetrdf;
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