@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP47224.RAV33a4g2clB3alxtsIkCjaZfeePIpCxTjiII-nV_sDw4> .
@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:NP47224.RAV33a4g2clB3alxtsIkCjaZfeePIpCxTjiII-nV_sDw4130_head {
  this: np:hasAssertion dgn-np:NP47224.RAV33a4g2clB3alxtsIkCjaZfeePIpCxTjiII-nV_sDw4130_assertion;
    np:hasProvenance dgn-np:NP47224.RAV33a4g2clB3alxtsIkCjaZfeePIpCxTjiII-nV_sDw4130_provenance;
    np:hasPublicationInfo dgn-np:NP47224.RAV33a4g2clB3alxtsIkCjaZfeePIpCxTjiII-nV_sDw4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP47224.RAV33a4g2clB3alxtsIkCjaZfeePIpCxTjiII-nV_sDw4130_assertion a np:Assertion .
  
  dgn-np:NP47224.RAV33a4g2clB3alxtsIkCjaZfeePIpCxTjiII-nV_sDw4130_provenance a np:Provenance .
  
  dgn-np:NP47224.RAV33a4g2clB3alxtsIkCjaZfeePIpCxTjiII-nV_sDw4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP47224.RAV33a4g2clB3alxtsIkCjaZfeePIpCxTjiII-nV_sDw4130_assertion {
  miriam-gene:1234 a ncit:C16612 .
  
  lld:C0002395 a ncit:C7057 .
  
  dgn-gda:DGNb375ad7457ba4413e1f65d625b317d51 sio:SIO_000628 miriam-gene:1234, lld:C0002395;
    a sio:SIO_001122 .
}

dgn-np:NP47224.RAV33a4g2clB3alxtsIkCjaZfeePIpCxTjiII-nV_sDw4130_provenance {
  dgn-np:NP47224.RAV33a4g2clB3alxtsIkCjaZfeePIpCxTjiII-nV_sDw4130_assertion dcterms:description
      "[However, these findings must be cautiously interpreted as the overall significance was found without adjustment for multiple comparisons and is coming from the complete absence of the genotype 64I/64I in AD patients. Conversely, no different distribution of the CCR5Delta32 deletion in the two populations was shown. Stratifying by the presence of ApoE varepsilon4 allele, gender or age at onset, no differences in either allele frequencies were observed.]. 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:15465089;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP47224.RAV33a4g2clB3alxtsIkCjaZfeePIpCxTjiII-nV_sDw4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:21+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" .
}