@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP901181.RAJOQOGTLfrayfPr09RrfekgUpGEwXX7TJjHO_VLizW4I> .
@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:NP901181.RAJOQOGTLfrayfPr09RrfekgUpGEwXX7TJjHO_VLizW4I130_head {
  this: np:hasAssertion dgn-np:NP901181.RAJOQOGTLfrayfPr09RrfekgUpGEwXX7TJjHO_VLizW4I130_assertion;
    np:hasProvenance dgn-np:NP901181.RAJOQOGTLfrayfPr09RrfekgUpGEwXX7TJjHO_VLizW4I130_provenance;
    np:hasPublicationInfo dgn-np:NP901181.RAJOQOGTLfrayfPr09RrfekgUpGEwXX7TJjHO_VLizW4I130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP901181.RAJOQOGTLfrayfPr09RrfekgUpGEwXX7TJjHO_VLizW4I130_assertion a np:Assertion .
  
  dgn-np:NP901181.RAJOQOGTLfrayfPr09RrfekgUpGEwXX7TJjHO_VLizW4I130_provenance a np:Provenance .
  
  dgn-np:NP901181.RAJOQOGTLfrayfPr09RrfekgUpGEwXX7TJjHO_VLizW4I130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP901181.RAJOQOGTLfrayfPr09RrfekgUpGEwXX7TJjHO_VLizW4I130_assertion {
  miriam-gene:6462 a ncit:C16612 .
  
  lld:C0038454 a ncit:C7057 .
  
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    a sio:SIO_001121 .
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dgn-np:NP901181.RAJOQOGTLfrayfPr09RrfekgUpGEwXX7TJjHO_VLizW4I130_provenance {
  dgn-np:NP901181.RAJOQOGTLfrayfPr09RrfekgUpGEwXX7TJjHO_VLizW4I130_assertion dcterms:description
      "[Discriminant function tests yielded baseline SBP, DBP, smoking, and parental history of stroke or hypertension to be the most significant precursors distinguishing hypertensive from normotensive groups, and the model correctly classified 69.7% of the subjects.]. 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:4036789;
    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:NP901181.RAJOQOGTLfrayfPr09RrfekgUpGEwXX7TJjHO_VLizW4I130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:13+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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