@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP72990.RAbHE-1TbXb9_xvP6LYQDblpDwHwS8q6KKEEtvI0PtKVY> .
@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:NP72990.RAbHE-1TbXb9_xvP6LYQDblpDwHwS8q6KKEEtvI0PtKVY130_head {
  this: np:hasAssertion dgn-np:NP72990.RAbHE-1TbXb9_xvP6LYQDblpDwHwS8q6KKEEtvI0PtKVY130_assertion;
    np:hasProvenance dgn-np:NP72990.RAbHE-1TbXb9_xvP6LYQDblpDwHwS8q6KKEEtvI0PtKVY130_provenance;
    np:hasPublicationInfo dgn-np:NP72990.RAbHE-1TbXb9_xvP6LYQDblpDwHwS8q6KKEEtvI0PtKVY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP72990.RAbHE-1TbXb9_xvP6LYQDblpDwHwS8q6KKEEtvI0PtKVY130_assertion a np:Assertion .
  
  dgn-np:NP72990.RAbHE-1TbXb9_xvP6LYQDblpDwHwS8q6KKEEtvI0PtKVY130_provenance a np:Provenance .
  
  dgn-np:NP72990.RAbHE-1TbXb9_xvP6LYQDblpDwHwS8q6KKEEtvI0PtKVY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP72990.RAbHE-1TbXb9_xvP6LYQDblpDwHwS8q6KKEEtvI0PtKVY130_assertion {
  miriam-gene:3458 a ncit:C16612 .
  
  lld:C0007222 a ncit:C7057 .
  
  dgn-gda:DGNaca3c763cc985e4b68bc8f43cae38c30 sio:SIO_000628 miriam-gene:3458, lld:C0007222;
    a sio:SIO_001122 .
}

dgn-np:NP72990.RAbHE-1TbXb9_xvP6LYQDblpDwHwS8q6KKEEtvI0PtKVY130_provenance {
  dgn-np:NP72990.RAbHE-1TbXb9_xvP6LYQDblpDwHwS8q6KKEEtvI0PtKVY130_assertion dcterms:description
      "[No association attained genome-wide significance, but several intriguing findings emerged. Notably, we replicated associations of chromosome 9p21 with major CVD. Additional studies are needed to validate these results. Finding genetic variants associated with CVD may point to novel disease pathways and identify potential targeted preventive therapies.]. 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:17903304;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP72990.RAbHE-1TbXb9_xvP6LYQDblpDwHwS8q6KKEEtvI0PtKVY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:35+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" .
}