@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP442206.RAPodYSmVhymh0DUjjjCdCUXpWIFSpzEmylToxtSV3vhQ> .
@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:NP442206.RAPodYSmVhymh0DUjjjCdCUXpWIFSpzEmylToxtSV3vhQ130_head {
  this: np:hasAssertion dgn-np:NP442206.RAPodYSmVhymh0DUjjjCdCUXpWIFSpzEmylToxtSV3vhQ130_assertion;
    np:hasProvenance dgn-np:NP442206.RAPodYSmVhymh0DUjjjCdCUXpWIFSpzEmylToxtSV3vhQ130_provenance;
    np:hasPublicationInfo dgn-np:NP442206.RAPodYSmVhymh0DUjjjCdCUXpWIFSpzEmylToxtSV3vhQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP442206.RAPodYSmVhymh0DUjjjCdCUXpWIFSpzEmylToxtSV3vhQ130_assertion a np:Assertion .
  
  dgn-np:NP442206.RAPodYSmVhymh0DUjjjCdCUXpWIFSpzEmylToxtSV3vhQ130_provenance a np:Provenance .
  
  dgn-np:NP442206.RAPodYSmVhymh0DUjjjCdCUXpWIFSpzEmylToxtSV3vhQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP442206.RAPodYSmVhymh0DUjjjCdCUXpWIFSpzEmylToxtSV3vhQ130_assertion {
  miriam-gene:3811 a ncit:C16612 .
  
  lld:C0086525 a ncit:C7057 .
  
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    a sio:SIO_001121 .
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dgn-np:NP442206.RAPodYSmVhymh0DUjjjCdCUXpWIFSpzEmylToxtSV3vhQ130_provenance {
  dgn-np:NP442206.RAPodYSmVhymh0DUjjjCdCUXpWIFSpzEmylToxtSV3vhQ130_assertion dcterms:description
      "[A comparison of several statistical methods and measures (gene frequency, haplotype frequency, and linkage disequilibrium estimation) using the Centre d'Etude du Polymorphisme Humain data will be provided using KIR haplotypes that have been determined by segregation analysis, noting the strengths and weaknesses of the methods when only the presence/absence data is considered.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
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    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 .
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dgn-np:NP442206.RAPodYSmVhymh0DUjjjCdCUXpWIFSpzEmylToxtSV3vhQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:23+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;
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    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
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