@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP412400.RAT-Jos2GBQVBLLSHRSnCcK4HLqLcg80H7u1rvqd2-V1M> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP412400.RAT-Jos2GBQVBLLSHRSnCcK4HLqLcg80H7u1rvqd2-V1M130_head {
  this: np:hasAssertion dgn-np:NP412400.RAT-Jos2GBQVBLLSHRSnCcK4HLqLcg80H7u1rvqd2-V1M130_assertion;
    np:hasProvenance dgn-np:NP412400.RAT-Jos2GBQVBLLSHRSnCcK4HLqLcg80H7u1rvqd2-V1M130_provenance;
    np:hasPublicationInfo dgn-np:NP412400.RAT-Jos2GBQVBLLSHRSnCcK4HLqLcg80H7u1rvqd2-V1M130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP412400.RAT-Jos2GBQVBLLSHRSnCcK4HLqLcg80H7u1rvqd2-V1M130_assertion a np:Assertion .
  
  dgn-np:NP412400.RAT-Jos2GBQVBLLSHRSnCcK4HLqLcg80H7u1rvqd2-V1M130_provenance a np:Provenance .
  
  dgn-np:NP412400.RAT-Jos2GBQVBLLSHRSnCcK4HLqLcg80H7u1rvqd2-V1M130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP412400.RAT-Jos2GBQVBLLSHRSnCcK4HLqLcg80H7u1rvqd2-V1M130_assertion {
  miriam-gene:2477 a ncit:C16612 .
  
  lld:C0004138 a ncit:C7057 .
  
  dgn-gda:DGNcbfb411abbd0d561d3581e206952410c sio:SIO_000628 miriam-gene:2477, lld:C0004138;
    a sio:SIO_001121 .
}

dgn-np:NP412400.RAT-Jos2GBQVBLLSHRSnCcK4HLqLcg80H7u1rvqd2-V1M130_provenance {
  dgn-np:NP412400.RAT-Jos2GBQVBLLSHRSnCcK4HLqLcg80H7u1rvqd2-V1M130_assertion dcterms:description
      "[Changes in a long list of additional genes have been suggested as causes for parkinsonism or PD, including genes for hereditary ataxias (ATXN2, ATXN3, FMR1), frontotemporal dementia (C9ORF72, GRN, MAPT, TARDBP), DYT5 (GCH1, TH, SPR), and others (ATP13A2, CSF1R, DNAJC6, FBXO, GIGYF2, HTRA2, PLA2G6, POLG, SPG11, UCHL1).]. 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:23462481;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP412400.RAT-Jos2GBQVBLLSHRSnCcK4HLqLcg80H7u1rvqd2-V1M130_publicationInfo {
  this: dcterms:created "2015-08-25T14:41:40+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}