@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP593117.RATkJR_4_qBHOHAQSmHfC7YBJ9abrKy1_XNVcO3Ow6Xls> .
@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:NP593117.RATkJR_4_qBHOHAQSmHfC7YBJ9abrKy1_XNVcO3Ow6Xls130_head {
  this: np:hasAssertion dgn-np:NP593117.RATkJR_4_qBHOHAQSmHfC7YBJ9abrKy1_XNVcO3Ow6Xls130_assertion;
    np:hasProvenance dgn-np:NP593117.RATkJR_4_qBHOHAQSmHfC7YBJ9abrKy1_XNVcO3Ow6Xls130_provenance;
    np:hasPublicationInfo dgn-np:NP593117.RATkJR_4_qBHOHAQSmHfC7YBJ9abrKy1_XNVcO3Ow6Xls130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP593117.RATkJR_4_qBHOHAQSmHfC7YBJ9abrKy1_XNVcO3Ow6Xls130_assertion a np:Assertion .
  
  dgn-np:NP593117.RATkJR_4_qBHOHAQSmHfC7YBJ9abrKy1_XNVcO3Ow6Xls130_provenance a np:Provenance .
  
  dgn-np:NP593117.RATkJR_4_qBHOHAQSmHfC7YBJ9abrKy1_XNVcO3Ow6Xls130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP593117.RATkJR_4_qBHOHAQSmHfC7YBJ9abrKy1_XNVcO3Ow6Xls130_assertion {
  miriam-gene:6584 a ncit:C16612 .
  
  lld:C0271287 a ncit:C7057 .
  
  dgn-gda:DGNf12190f0f8bf6fa6eb71da77eb9fe076 sio:SIO_000628 miriam-gene:6584, lld:C0271287;
    a sio:SIO_001121 .
}

dgn-np:NP593117.RATkJR_4_qBHOHAQSmHfC7YBJ9abrKy1_XNVcO3Ow6Xls130_provenance {
  dgn-np:NP593117.RATkJR_4_qBHOHAQSmHfC7YBJ9abrKy1_XNVcO3Ow6Xls130_assertion dcterms:description
      "[In this review, we examine the evidence for genetic susceptibility to SCD in order to provide biological insight into the pathogenesis of this devastating disease and to explore the potential for genetics to impact clinical management of SCD risk.]. 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:22703174;
    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:NP593117.RATkJR_4_qBHOHAQSmHfC7YBJ9abrKy1_XNVcO3Ow6Xls130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:56+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" .
}