@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP267772.RAzJ5RcafTOysZZoS0k2xZZn9SN19osGfuulO44ohC-nY> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP267772.RAzJ5RcafTOysZZoS0k2xZZn9SN19osGfuulO44ohC-nY130_head {
  this: np:hasAssertion dgn-np:NP267772.RAzJ5RcafTOysZZoS0k2xZZn9SN19osGfuulO44ohC-nY130_assertion;
    np:hasProvenance dgn-np:NP267772.RAzJ5RcafTOysZZoS0k2xZZn9SN19osGfuulO44ohC-nY130_provenance;
    np:hasPublicationInfo dgn-np:NP267772.RAzJ5RcafTOysZZoS0k2xZZn9SN19osGfuulO44ohC-nY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP267772.RAzJ5RcafTOysZZoS0k2xZZn9SN19osGfuulO44ohC-nY130_assertion a np:Assertion .
  
  dgn-np:NP267772.RAzJ5RcafTOysZZoS0k2xZZn9SN19osGfuulO44ohC-nY130_provenance a np:Provenance .
  
  dgn-np:NP267772.RAzJ5RcafTOysZZoS0k2xZZn9SN19osGfuulO44ohC-nY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP267772.RAzJ5RcafTOysZZoS0k2xZZn9SN19osGfuulO44ohC-nY130_assertion {
  miriam-gene:635 a ncit:C16612 .
  
  lld:C0948008 a ncit:C7057 .
  
  dgn-gda:DGNcbac3edf3b04d47b11b3cb2083850dfd sio:SIO_000628 miriam-gene:635, lld:C0948008;
    a sio:SIO_001121 .
}

dgn-np:NP267772.RAzJ5RcafTOysZZoS0k2xZZn9SN19osGfuulO44ohC-nY130_provenance {
  dgn-np:NP267772.RAzJ5RcafTOysZZoS0k2xZZn9SN19osGfuulO44ohC-nY130_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-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP267772.RAzJ5RcafTOysZZoS0k2xZZn9SN19osGfuulO44ohC-nY130_publicationInfo {
  this: dcterms:created "2015-08-25T14:40:12+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}