@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP812667.RAVRsiYqjUuVCNA5oBJEHnO_Vj9Bxh7_pE-M3kOQNgAnw> .
@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:NP812667.RAVRsiYqjUuVCNA5oBJEHnO_Vj9Bxh7_pE-M3kOQNgAnw130_head {
  this: np:hasAssertion dgn-np:NP812667.RAVRsiYqjUuVCNA5oBJEHnO_Vj9Bxh7_pE-M3kOQNgAnw130_assertion;
    np:hasProvenance dgn-np:NP812667.RAVRsiYqjUuVCNA5oBJEHnO_Vj9Bxh7_pE-M3kOQNgAnw130_provenance;
    np:hasPublicationInfo dgn-np:NP812667.RAVRsiYqjUuVCNA5oBJEHnO_Vj9Bxh7_pE-M3kOQNgAnw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP812667.RAVRsiYqjUuVCNA5oBJEHnO_Vj9Bxh7_pE-M3kOQNgAnw130_assertion a np:Assertion .
  
  dgn-np:NP812667.RAVRsiYqjUuVCNA5oBJEHnO_Vj9Bxh7_pE-M3kOQNgAnw130_provenance a np:Provenance .
  
  dgn-np:NP812667.RAVRsiYqjUuVCNA5oBJEHnO_Vj9Bxh7_pE-M3kOQNgAnw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP812667.RAVRsiYqjUuVCNA5oBJEHnO_Vj9Bxh7_pE-M3kOQNgAnw130_assertion {
  miriam-gene:6403 a ncit:C16612 .
  
  lld:C0020443 a ncit:C7057 .
  
  dgn-gda:DGNf38309470689467c1cc162c04d3df6ea sio:SIO_000628 miriam-gene:6403, lld:C0020443;
    a sio:SIO_001121 .
}

dgn-np:NP812667.RAVRsiYqjUuVCNA5oBJEHnO_Vj9Bxh7_pE-M3kOQNgAnw130_provenance {
  dgn-np:NP812667.RAVRsiYqjUuVCNA5oBJEHnO_Vj9Bxh7_pE-M3kOQNgAnw130_assertion dcterms:description
      "[There was no significant association between conventional risk factors (such as hypercholesterolaemia, increased body mass index, or raised blood pressure) and either the rare or the common Pro(715) allele of the P-selectin gene in controls.]. 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:11040019;
    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:NP812667.RAVRsiYqjUuVCNA5oBJEHnO_Vj9Bxh7_pE-M3kOQNgAnw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:18+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" .
}