@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP280498.RAAMw2fJdNbMupu4_ZXQxzKs_sePH1iqDPml0-7oRJ7Gk> .
@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:NP280498.RAAMw2fJdNbMupu4_ZXQxzKs_sePH1iqDPml0-7oRJ7Gk130_head {
  this: np:hasAssertion dgn-np:NP280498.RAAMw2fJdNbMupu4_ZXQxzKs_sePH1iqDPml0-7oRJ7Gk130_assertion;
    np:hasProvenance dgn-np:NP280498.RAAMw2fJdNbMupu4_ZXQxzKs_sePH1iqDPml0-7oRJ7Gk130_provenance;
    np:hasPublicationInfo dgn-np:NP280498.RAAMw2fJdNbMupu4_ZXQxzKs_sePH1iqDPml0-7oRJ7Gk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP280498.RAAMw2fJdNbMupu4_ZXQxzKs_sePH1iqDPml0-7oRJ7Gk130_assertion a np:Assertion .
  
  dgn-np:NP280498.RAAMw2fJdNbMupu4_ZXQxzKs_sePH1iqDPml0-7oRJ7Gk130_provenance a np:Provenance .
  
  dgn-np:NP280498.RAAMw2fJdNbMupu4_ZXQxzKs_sePH1iqDPml0-7oRJ7Gk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP280498.RAAMw2fJdNbMupu4_ZXQxzKs_sePH1iqDPml0-7oRJ7Gk130_assertion {
  miriam-gene:4137 a ncit:C16612 .
  
  lld:C0524851 a ncit:C7057 .
  
  dgn-gda:DGN682562c2c254bb8f12cf367e860c078f sio:SIO_000628 miriam-gene:4137, lld:C0524851;
    a sio:SIO_001121 .
}

dgn-np:NP280498.RAAMw2fJdNbMupu4_ZXQxzKs_sePH1iqDPml0-7oRJ7Gk130_provenance {
  dgn-np:NP280498.RAAMw2fJdNbMupu4_ZXQxzKs_sePH1iqDPml0-7oRJ7Gk130_assertion dcterms:description
      "[Frontotemporal dementia is commonly associated with parkinsonism in several sporadic (i.e., progressive supranuclear palsy, corticobasal degeneration) and familial neurodegenerative disorders (i.e., frontotemporal dementia associated with parkinsonism and MAPT or progranulin mutations in chromosome 17).]. 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:21892619;
    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:NP280498.RAAMw2fJdNbMupu4_ZXQxzKs_sePH1iqDPml0-7oRJ7Gk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:38+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" .
}