@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP290734.RAH78uf9ipXVxvaSCKNq-R0eq3tGLDEPF-UQUaejOfHTg> .
@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:NP290734.RAH78uf9ipXVxvaSCKNq-R0eq3tGLDEPF-UQUaejOfHTg130_head {
  this: np:hasAssertion dgn-np:NP290734.RAH78uf9ipXVxvaSCKNq-R0eq3tGLDEPF-UQUaejOfHTg130_assertion;
    np:hasProvenance dgn-np:NP290734.RAH78uf9ipXVxvaSCKNq-R0eq3tGLDEPF-UQUaejOfHTg130_provenance;
    np:hasPublicationInfo dgn-np:NP290734.RAH78uf9ipXVxvaSCKNq-R0eq3tGLDEPF-UQUaejOfHTg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP290734.RAH78uf9ipXVxvaSCKNq-R0eq3tGLDEPF-UQUaejOfHTg130_assertion a np:Assertion .
  
  dgn-np:NP290734.RAH78uf9ipXVxvaSCKNq-R0eq3tGLDEPF-UQUaejOfHTg130_provenance a np:Provenance .
  
  dgn-np:NP290734.RAH78uf9ipXVxvaSCKNq-R0eq3tGLDEPF-UQUaejOfHTg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP290734.RAH78uf9ipXVxvaSCKNq-R0eq3tGLDEPF-UQUaejOfHTg130_assertion {
  miriam-gene:57379 a ncit:C16612 .
  
  lld:C1306589 a ncit:C7057 .
  
  dgn-gda:DGN3d6236cf14effa9d550eb9de742a48e7 sio:SIO_000628 miriam-gene:57379, lld:C1306589;
    a sio:SIO_001121 .
}

dgn-np:NP290734.RAH78uf9ipXVxvaSCKNq-R0eq3tGLDEPF-UQUaejOfHTg130_provenance {
  dgn-np:NP290734.RAH78uf9ipXVxvaSCKNq-R0eq3tGLDEPF-UQUaejOfHTg130_assertion dcterms:description
      "[After the identification of the locus for CDA II, also known as HEMPAS (hereditary erythroblast multinuclearity with positive acidified serum test), on the long arm of chromosome 20 (20q11.2) we have analyzed by a mutational search seven candidate genes in a large series of CDA II patients.]. 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:12667984;
    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:NP290734.RAH78uf9ipXVxvaSCKNq-R0eq3tGLDEPF-UQUaejOfHTg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:45+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" .
}