@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP874744.RAGWys4ChXFhTf0TCojGuqUT-Iat_ahTgd0fkzGdCntaE> .
@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:NP874744.RAGWys4ChXFhTf0TCojGuqUT-Iat_ahTgd0fkzGdCntaE130_head {
  this: np:hasAssertion dgn-np:NP874744.RAGWys4ChXFhTf0TCojGuqUT-Iat_ahTgd0fkzGdCntaE130_assertion;
    np:hasProvenance dgn-np:NP874744.RAGWys4ChXFhTf0TCojGuqUT-Iat_ahTgd0fkzGdCntaE130_provenance;
    np:hasPublicationInfo dgn-np:NP874744.RAGWys4ChXFhTf0TCojGuqUT-Iat_ahTgd0fkzGdCntaE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP874744.RAGWys4ChXFhTf0TCojGuqUT-Iat_ahTgd0fkzGdCntaE130_assertion a np:Assertion .
  
  dgn-np:NP874744.RAGWys4ChXFhTf0TCojGuqUT-Iat_ahTgd0fkzGdCntaE130_provenance a np:Provenance .
  
  dgn-np:NP874744.RAGWys4ChXFhTf0TCojGuqUT-Iat_ahTgd0fkzGdCntaE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP874744.RAGWys4ChXFhTf0TCojGuqUT-Iat_ahTgd0fkzGdCntaE130_assertion {
  miriam-gene:1659 a ncit:C16612 .
  
  lld:C1956346 a ncit:C7057 .
  
  dgn-gda:DGN8c37819a34e5a7f9f4c04e81bb3ee647 sio:SIO_000628 miriam-gene:1659, lld:C1956346;
    a sio:SIO_001121 .
}

dgn-np:NP874744.RAGWys4ChXFhTf0TCojGuqUT-Iat_ahTgd0fkzGdCntaE130_provenance {
  dgn-np:NP874744.RAGWys4ChXFhTf0TCojGuqUT-Iat_ahTgd0fkzGdCntaE130_assertion dcterms:description
      "[We did not find any evidence of association of the two novel SNPs in MDM4 and HRH1 with sequelae of high BP including coronary artery disease (CAD), left ventricular hypertrophy (LVH) or stroke.]. 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:23303523;
    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:NP874744.RAGWys4ChXFhTf0TCojGuqUT-Iat_ahTgd0fkzGdCntaE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:54+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" .
}