@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP262743.RAtUQjsyBWRT8fEN4utrMhkcibpat5ZeTh_BtykLZy5vs> .
@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:NP262743.RAtUQjsyBWRT8fEN4utrMhkcibpat5ZeTh_BtykLZy5vs130_head {
  this: np:hasAssertion dgn-np:NP262743.RAtUQjsyBWRT8fEN4utrMhkcibpat5ZeTh_BtykLZy5vs130_assertion;
    np:hasProvenance dgn-np:NP262743.RAtUQjsyBWRT8fEN4utrMhkcibpat5ZeTh_BtykLZy5vs130_provenance;
    np:hasPublicationInfo dgn-np:NP262743.RAtUQjsyBWRT8fEN4utrMhkcibpat5ZeTh_BtykLZy5vs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP262743.RAtUQjsyBWRT8fEN4utrMhkcibpat5ZeTh_BtykLZy5vs130_assertion a np:Assertion .
  
  dgn-np:NP262743.RAtUQjsyBWRT8fEN4utrMhkcibpat5ZeTh_BtykLZy5vs130_provenance a np:Provenance .
  
  dgn-np:NP262743.RAtUQjsyBWRT8fEN4utrMhkcibpat5ZeTh_BtykLZy5vs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP262743.RAtUQjsyBWRT8fEN4utrMhkcibpat5ZeTh_BtykLZy5vs130_assertion {
  miriam-gene:6948 a ncit:C16612 .
  
  lld:C0948008 a ncit:C7057 .
  
  dgn-gda:DGN6ea9387bb5084633b4856853218e7d5a sio:SIO_000628 miriam-gene:6948, lld:C0948008;
    a sio:SIO_001121 .
}

dgn-np:NP262743.RAtUQjsyBWRT8fEN4utrMhkcibpat5ZeTh_BtykLZy5vs130_provenance {
  dgn-np:NP262743.RAtUQjsyBWRT8fEN4utrMhkcibpat5ZeTh_BtykLZy5vs130_assertion dcterms:description
      "[After haplotype reconstruction, generalised linear model analyses adjusted for traditional risk factors and using the FDR multiple testing correction showed significant associations between ischaemic stroke and BHMT, CBS, FOLH1, MTR, PON2, TCN2 and TYMS haplotypes.]. 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:20458436;
    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:NP262743.RAtUQjsyBWRT8fEN4utrMhkcibpat5ZeTh_BtykLZy5vs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:27+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" .
}