@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP175186.RACMRrhOK9JMdwHEOKQPIC3hx4yq3cpXbhabGjRaQdFHY> .
@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 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:NP175186.RACMRrhOK9JMdwHEOKQPIC3hx4yq3cpXbhabGjRaQdFHY130_head {
   this: np:hasAssertion dgn-np:NP175186.RACMRrhOK9JMdwHEOKQPIC3hx4yq3cpXbhabGjRaQdFHY130_assertion ;
    np:hasProvenance dgn-np:NP175186.RACMRrhOK9JMdwHEOKQPIC3hx4yq3cpXbhabGjRaQdFHY130_provenance ;
    np:hasPublicationInfo dgn-np:NP175186.RACMRrhOK9JMdwHEOKQPIC3hx4yq3cpXbhabGjRaQdFHY130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP175186.RACMRrhOK9JMdwHEOKQPIC3hx4yq3cpXbhabGjRaQdFHY130_assertion a np:Assertion .
  dgn-np:NP175186.RACMRrhOK9JMdwHEOKQPIC3hx4yq3cpXbhabGjRaQdFHY130_provenance a np:Provenance .
  dgn-np:NP175186.RACMRrhOK9JMdwHEOKQPIC3hx4yq3cpXbhabGjRaQdFHY130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP175186.RACMRrhOK9JMdwHEOKQPIC3hx4yq3cpXbhabGjRaQdFHY130_assertion {
   miriam-gene:10249 a ncit:C16612 .
  lld:C0024530 a ncit:C7057 .
  dgn-gda:DGN4f10f14886447dae0d1fd3d21ea1c602 sio:SIO_000628 miriam-gene:10249 , lld:C0024530 ;
    a sio:SIO_001121 .
}
dgn-np:NP175186.RACMRrhOK9JMdwHEOKQPIC3hx4yq3cpXbhabGjRaQdFHY130_provenance {
   dgn-np:NP175186.RACMRrhOK9JMdwHEOKQPIC3hx4yq3cpXbhabGjRaQdFHY130_assertion dct:description "[Further, the overall haplotype analysis for all the three loci showed predominantly two major haplotypes 'AAC' coding for higher expression of CR1 and 'TGG' haplotype coding for low expression of CR1 level with the former haplotype being significantly associated with CM (P value<0.00619 after Bonferroni correction) compared to mild malaria.]. 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:20951238 ;
    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:NP175186.RACMRrhOK9JMdwHEOKQPIC3hx4yq3cpXbhabGjRaQdFHY130_publicationInfo {
   this: dct:created "2014-10-02T12:33:34+02:00"^^xsd:dateTime ;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dct:rightsHolder dgn-void:IBIGroup ;
    dct:subject sio:SIO_000983 ;
    prv:usedData dgn-void:disgenetrdf ;
    pav:authoredBy orcid:0000-0001-5999-6269 , orcid:0000-0002-7534-7661 , orcid:0000-0002-9383-528X , orcid:0000-0003-0169-8159 , orcid:0000-0003-1244-7654 ;
    pav:createdBy orcid:0000-0003-0169-8159 ;
    pav:version "v2.1.0.0" .
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}