@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP373317.RAE-ELkeqSX1L7s09EsxisLj1hl1wyUgAykdYDnNAU_WI> .
@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:NP373317.RAE-ELkeqSX1L7s09EsxisLj1hl1wyUgAykdYDnNAU_WI130_head {
  this: np:hasAssertion dgn-np:NP373317.RAE-ELkeqSX1L7s09EsxisLj1hl1wyUgAykdYDnNAU_WI130_assertion;
    np:hasProvenance dgn-np:NP373317.RAE-ELkeqSX1L7s09EsxisLj1hl1wyUgAykdYDnNAU_WI130_provenance;
    np:hasPublicationInfo dgn-np:NP373317.RAE-ELkeqSX1L7s09EsxisLj1hl1wyUgAykdYDnNAU_WI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP373317.RAE-ELkeqSX1L7s09EsxisLj1hl1wyUgAykdYDnNAU_WI130_assertion a np:Assertion .
  
  dgn-np:NP373317.RAE-ELkeqSX1L7s09EsxisLj1hl1wyUgAykdYDnNAU_WI130_provenance a np:Provenance .
  
  dgn-np:NP373317.RAE-ELkeqSX1L7s09EsxisLj1hl1wyUgAykdYDnNAU_WI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP373317.RAE-ELkeqSX1L7s09EsxisLj1hl1wyUgAykdYDnNAU_WI130_assertion {
  miriam-gene:2395 a ncit:C16612 .
  
  lld:C0007194 a ncit:C7057 .
  
  dgn-gda:DGN636c93a56338e88e06513a31c215ae7c sio:SIO_000628 miriam-gene:2395, lld:C0007194;
    a sio:SIO_001121 .
}

dgn-np:NP373317.RAE-ELkeqSX1L7s09EsxisLj1hl1wyUgAykdYDnNAU_WI130_provenance {
  dgn-np:NP373317.RAE-ELkeqSX1L7s09EsxisLj1hl1wyUgAykdYDnNAU_WI130_assertion dcterms:description
      "[The observation that some patients with only mild-to-moderate hypertension exhibit gross left ventricular hypertrophy (LVH) similar to the inherited hypertrophic cardiomyopathies such as familial hypertrophic cardiomyopathy (FHC) and Friedreich's ataxia (FA) has prompted us to investigate the hypothesis that genetic factors associated with excessive myocardial hypertrophy, viz.]. 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:8807151;
    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:NP373317.RAE-ELkeqSX1L7s09EsxisLj1hl1wyUgAykdYDnNAU_WI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:38+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" .
}