@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP489301.RA1HFC4nhRWLOmnFrHFLOpFxeLld9STvPUko0lfPXISQA> .
@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:NP489301.RA1HFC4nhRWLOmnFrHFLOpFxeLld9STvPUko0lfPXISQA130_head {
  this: np:hasAssertion dgn-np:NP489301.RA1HFC4nhRWLOmnFrHFLOpFxeLld9STvPUko0lfPXISQA130_assertion;
    np:hasProvenance dgn-np:NP489301.RA1HFC4nhRWLOmnFrHFLOpFxeLld9STvPUko0lfPXISQA130_provenance;
    np:hasPublicationInfo dgn-np:NP489301.RA1HFC4nhRWLOmnFrHFLOpFxeLld9STvPUko0lfPXISQA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP489301.RA1HFC4nhRWLOmnFrHFLOpFxeLld9STvPUko0lfPXISQA130_assertion a np:Assertion .
  
  dgn-np:NP489301.RA1HFC4nhRWLOmnFrHFLOpFxeLld9STvPUko0lfPXISQA130_provenance a np:Provenance .
  
  dgn-np:NP489301.RA1HFC4nhRWLOmnFrHFLOpFxeLld9STvPUko0lfPXISQA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP489301.RA1HFC4nhRWLOmnFrHFLOpFxeLld9STvPUko0lfPXISQA130_assertion {
  miriam-gene:1437 a ncit:C16612 .
  
  lld:C0752347 a ncit:C7057 .
  
  dgn-gda:DGN14bfcec7ae7ec45dbdaa63f1a5aa5852 sio:SIO_000628 miriam-gene:1437, lld:C0752347;
    a sio:SIO_001121 .
}

dgn-np:NP489301.RA1HFC4nhRWLOmnFrHFLOpFxeLld9STvPUko0lfPXISQA130_provenance {
  dgn-np:NP489301.RA1HFC4nhRWLOmnFrHFLOpFxeLld9STvPUko0lfPXISQA130_assertion dcterms:description
      "[The concept of PDD and DLB being separate conditions is comparatively new, and the most promising tools with which to separate them at present are cerebrospinal fluid (CSF) markers and positron emission tomography (PET) scanning that indicate increased amyloid-beta burden in DLB compared to PDD.]. 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:20338799;
    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:NP489301.RA1HFC4nhRWLOmnFrHFLOpFxeLld9STvPUko0lfPXISQA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:52+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" .
}