@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP615418.RAVOu4IT7mZMa_1qHED19gW9fxwj_I6vcvsbXSCcdPYT0> .
@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:NP615418.RAVOu4IT7mZMa_1qHED19gW9fxwj_I6vcvsbXSCcdPYT0130_head {
  this: np:hasAssertion dgn-np:NP615418.RAVOu4IT7mZMa_1qHED19gW9fxwj_I6vcvsbXSCcdPYT0130_assertion;
    np:hasProvenance dgn-np:NP615418.RAVOu4IT7mZMa_1qHED19gW9fxwj_I6vcvsbXSCcdPYT0130_provenance;
    np:hasPublicationInfo dgn-np:NP615418.RAVOu4IT7mZMa_1qHED19gW9fxwj_I6vcvsbXSCcdPYT0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP615418.RAVOu4IT7mZMa_1qHED19gW9fxwj_I6vcvsbXSCcdPYT0130_assertion a np:Assertion .
  
  dgn-np:NP615418.RAVOu4IT7mZMa_1qHED19gW9fxwj_I6vcvsbXSCcdPYT0130_provenance a np:Provenance .
  
  dgn-np:NP615418.RAVOu4IT7mZMa_1qHED19gW9fxwj_I6vcvsbXSCcdPYT0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP615418.RAVOu4IT7mZMa_1qHED19gW9fxwj_I6vcvsbXSCcdPYT0130_assertion {
  miriam-gene:4358 a ncit:C16612 .
  
  lld:C0037061 a ncit:C7057 .
  
  dgn-gda:DGNc69355227543fdcf60cfcd0ed6b97901 sio:SIO_000628 miriam-gene:4358, lld:C0037061;
    a sio:SIO_001121 .
}

dgn-np:NP615418.RAVOu4IT7mZMa_1qHED19gW9fxwj_I6vcvsbXSCcdPYT0130_provenance {
  dgn-np:NP615418.RAVOu4IT7mZMa_1qHED19gW9fxwj_I6vcvsbXSCcdPYT0130_assertion dcterms:description
      "[SS mice were similar to humans with sickle cell disease in having erythrocytic sickling, vascular ectasia, intravascular hemolysis, exuberant hematopoiesis, cardiomegaly, glomerulosclerosis, visceral congestion, hemorrhages, multiorgan infarcts, pyknotic neurons, and progressive siderosis.]. 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:16166585;
    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:NP615418.RAVOu4IT7mZMa_1qHED19gW9fxwj_I6vcvsbXSCcdPYT0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:12+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" .
}