@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP527949.RAS67SI3ZS03RE1De3PJK-6dw2RdUlZCQQKd8X4HdHCVU> .
@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:NP527949.RAS67SI3ZS03RE1De3PJK-6dw2RdUlZCQQKd8X4HdHCVU130_head {
  this: np:hasAssertion dgn-np:NP527949.RAS67SI3ZS03RE1De3PJK-6dw2RdUlZCQQKd8X4HdHCVU130_assertion;
    np:hasProvenance dgn-np:NP527949.RAS67SI3ZS03RE1De3PJK-6dw2RdUlZCQQKd8X4HdHCVU130_provenance;
    np:hasPublicationInfo dgn-np:NP527949.RAS67SI3ZS03RE1De3PJK-6dw2RdUlZCQQKd8X4HdHCVU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP527949.RAS67SI3ZS03RE1De3PJK-6dw2RdUlZCQQKd8X4HdHCVU130_assertion a np:Assertion .
  
  dgn-np:NP527949.RAS67SI3ZS03RE1De3PJK-6dw2RdUlZCQQKd8X4HdHCVU130_provenance a np:Provenance .
  
  dgn-np:NP527949.RAS67SI3ZS03RE1De3PJK-6dw2RdUlZCQQKd8X4HdHCVU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP527949.RAS67SI3ZS03RE1De3PJK-6dw2RdUlZCQQKd8X4HdHCVU130_assertion {
  miriam-gene:3342 a ncit:C16612 .
  
  lld:C0678236 a ncit:C7057 .
  
  dgn-gda:DGNc6c900e57af1924649d012743ca0c413 sio:SIO_000628 miriam-gene:3342, lld:C0678236;
    a sio:SIO_001121 .
}

dgn-np:NP527949.RAS67SI3ZS03RE1De3PJK-6dw2RdUlZCQQKd8X4HdHCVU130_provenance {
  dgn-np:NP527949.RAS67SI3ZS03RE1De3PJK-6dw2RdUlZCQQKd8X4HdHCVU130_assertion dcterms:description
      "[METHODS Owing to the national array-CGH network funded by the French Ministry of Health, shared information about patients with rare disease helped to define critical intervals and evaluate their gene content, and finally determine the phenotypic consequences of genomic array findings.]. 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:20522426;
    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:NP527949.RAS67SI3ZS03RE1De3PJK-6dw2RdUlZCQQKd8X4HdHCVU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:19+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" .
}