@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP454549.RAusPLIieok4uhRAnOpTcGWUi9i39AqnQCNyM33hc8Ddc> .
@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:NP454549.RAusPLIieok4uhRAnOpTcGWUi9i39AqnQCNyM33hc8Ddc130_head {
  this: np:hasAssertion dgn-np:NP454549.RAusPLIieok4uhRAnOpTcGWUi9i39AqnQCNyM33hc8Ddc130_assertion;
    np:hasProvenance dgn-np:NP454549.RAusPLIieok4uhRAnOpTcGWUi9i39AqnQCNyM33hc8Ddc130_provenance;
    np:hasPublicationInfo dgn-np:NP454549.RAusPLIieok4uhRAnOpTcGWUi9i39AqnQCNyM33hc8Ddc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP454549.RAusPLIieok4uhRAnOpTcGWUi9i39AqnQCNyM33hc8Ddc130_assertion a np:Assertion .
  
  dgn-np:NP454549.RAusPLIieok4uhRAnOpTcGWUi9i39AqnQCNyM33hc8Ddc130_provenance a np:Provenance .
  
  dgn-np:NP454549.RAusPLIieok4uhRAnOpTcGWUi9i39AqnQCNyM33hc8Ddc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP454549.RAusPLIieok4uhRAnOpTcGWUi9i39AqnQCNyM33hc8Ddc130_assertion {
  miriam-gene:27034 a ncit:C16612 .
  
  lld:C0432306 a ncit:C7057 .
  
  dgn-gda:DGNf367d3339b652f0689e0eeaaf9b37f79 sio:SIO_000628 miriam-gene:27034, lld:C0432306;
    a sio:SIO_001121 .
}

dgn-np:NP454549.RAusPLIieok4uhRAnOpTcGWUi9i39AqnQCNyM33hc8Ddc130_provenance {
  dgn-np:NP454549.RAusPLIieok4uhRAnOpTcGWUi9i39AqnQCNyM33hc8Ddc130_assertion dcterms:description
      "[Therefore we applied the Combinatorial Mismatch Scanning (CMS) method that compares identity by state (IBS) (under the presumption of identity by descent (IBD)) sharing in distantly related individuals from such populations where standard linkage and association analyses are difficult to implement.]. 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:16515697;
    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:NP454549.RAusPLIieok4uhRAnOpTcGWUi9i39AqnQCNyM33hc8Ddc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:31+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" .
}