@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP672494.RAWlbjguYSljoIaLNI0hf1yuxeBwD19d6PDbXh7ts56f8> .
@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:NP672494.RAWlbjguYSljoIaLNI0hf1yuxeBwD19d6PDbXh7ts56f8130_head {
  this: np:hasAssertion dgn-np:NP672494.RAWlbjguYSljoIaLNI0hf1yuxeBwD19d6PDbXh7ts56f8130_assertion;
    np:hasProvenance dgn-np:NP672494.RAWlbjguYSljoIaLNI0hf1yuxeBwD19d6PDbXh7ts56f8130_provenance;
    np:hasPublicationInfo dgn-np:NP672494.RAWlbjguYSljoIaLNI0hf1yuxeBwD19d6PDbXh7ts56f8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP672494.RAWlbjguYSljoIaLNI0hf1yuxeBwD19d6PDbXh7ts56f8130_assertion a np:Assertion .
  
  dgn-np:NP672494.RAWlbjguYSljoIaLNI0hf1yuxeBwD19d6PDbXh7ts56f8130_provenance a np:Provenance .
  
  dgn-np:NP672494.RAWlbjguYSljoIaLNI0hf1yuxeBwD19d6PDbXh7ts56f8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP672494.RAWlbjguYSljoIaLNI0hf1yuxeBwD19d6PDbXh7ts56f8130_assertion {
  miriam-gene:26047 a ncit:C16612 .
  
  lld:C0751396 a ncit:C7057 .
  
  dgn-gda:DGN763956d8f82440ccd6c8dc039d314514 sio:SIO_000628 miriam-gene:26047, lld:C0751396;
    a sio:SIO_001121 .
}

dgn-np:NP672494.RAWlbjguYSljoIaLNI0hf1yuxeBwD19d6PDbXh7ts56f8130_provenance {
  dgn-np:NP672494.RAWlbjguYSljoIaLNI0hf1yuxeBwD19d6PDbXh7ts56f8130_assertion dcterms:description
      "[In a set of 25 glioblastomas and 22 oligodendrogliomas, mutation analysis identified two additional samples with genetic alterations in the CASPR2 gene and all three identified genetic alterations are likely to reduce CASPR2 protein expression levels.]. 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:20711234;
    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:NP672494.RAWlbjguYSljoIaLNI0hf1yuxeBwD19d6PDbXh7ts56f8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:46+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" .
}