@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP136080.RA8tOymfKVb6E4ByG9y8yKOCQ3LNcMQGoMZ9vmDFZFAQ8> .
@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:NP136080.RA8tOymfKVb6E4ByG9y8yKOCQ3LNcMQGoMZ9vmDFZFAQ8130_head {
  this: np:hasAssertion dgn-np:NP136080.RA8tOymfKVb6E4ByG9y8yKOCQ3LNcMQGoMZ9vmDFZFAQ8130_assertion;
    np:hasProvenance dgn-np:NP136080.RA8tOymfKVb6E4ByG9y8yKOCQ3LNcMQGoMZ9vmDFZFAQ8130_provenance;
    np:hasPublicationInfo dgn-np:NP136080.RA8tOymfKVb6E4ByG9y8yKOCQ3LNcMQGoMZ9vmDFZFAQ8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP136080.RA8tOymfKVb6E4ByG9y8yKOCQ3LNcMQGoMZ9vmDFZFAQ8130_assertion a np:Assertion .
  
  dgn-np:NP136080.RA8tOymfKVb6E4ByG9y8yKOCQ3LNcMQGoMZ9vmDFZFAQ8130_provenance a np:Provenance .
  
  dgn-np:NP136080.RA8tOymfKVb6E4ByG9y8yKOCQ3LNcMQGoMZ9vmDFZFAQ8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP136080.RA8tOymfKVb6E4ByG9y8yKOCQ3LNcMQGoMZ9vmDFZFAQ8130_assertion {
  miriam-gene:3123 a ncit:C16612 .
  
  lld:C0002895 a ncit:C7057 .
  
  dgn-gda:DGN0478d11a3f75409f12dad4968f30bee2 sio:SIO_000628 miriam-gene:3123, lld:C0002895;
    a sio:SIO_001122 .
}

dgn-np:NP136080.RA8tOymfKVb6E4ByG9y8yKOCQ3LNcMQGoMZ9vmDFZFAQ8130_provenance {
  dgn-np:NP136080.RA8tOymfKVb6E4ByG9y8yKOCQ3LNcMQGoMZ9vmDFZFAQ8130_assertion dcterms:description
      "[results show that specific HLA haplotypes influence sickle cell anemia (SCA) osteomyelitis risk and that specific HLA types may serve as markers for identifying SCA patients at high risk for osteomyelitis ]. 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:18312480;
    prov:wasDerivedFrom dgn-void:lhgdn-20090331;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:lhgdn-20090331 pav:importedOn "2009-03-31"^^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:NP136080.RA8tOymfKVb6E4ByG9y8yKOCQ3LNcMQGoMZ9vmDFZFAQ8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:11+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" .
}