@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP836720.RAKZDByMw7xfYwLPYD2cNZk_z-5_7sBqO_0Dz2wFr4Kgs> .
@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:NP836720.RAKZDByMw7xfYwLPYD2cNZk_z-5_7sBqO_0Dz2wFr4Kgs130_head {
  this: np:hasAssertion dgn-np:NP836720.RAKZDByMw7xfYwLPYD2cNZk_z-5_7sBqO_0Dz2wFr4Kgs130_assertion;
    np:hasProvenance dgn-np:NP836720.RAKZDByMw7xfYwLPYD2cNZk_z-5_7sBqO_0Dz2wFr4Kgs130_provenance;
    np:hasPublicationInfo dgn-np:NP836720.RAKZDByMw7xfYwLPYD2cNZk_z-5_7sBqO_0Dz2wFr4Kgs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP836720.RAKZDByMw7xfYwLPYD2cNZk_z-5_7sBqO_0Dz2wFr4Kgs130_assertion a np:Assertion .
  
  dgn-np:NP836720.RAKZDByMw7xfYwLPYD2cNZk_z-5_7sBqO_0Dz2wFr4Kgs130_provenance a np:Provenance .
  
  dgn-np:NP836720.RAKZDByMw7xfYwLPYD2cNZk_z-5_7sBqO_0Dz2wFr4Kgs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP836720.RAKZDByMw7xfYwLPYD2cNZk_z-5_7sBqO_0Dz2wFr4Kgs130_assertion {
  miriam-gene:27129 a ncit:C16612 .
  
  lld:C1135191 a ncit:C7057 .
  
  dgn-gda:DGN2bc180dfa774afcf8a044a5c8a06934f sio:SIO_000628 miriam-gene:27129, lld:C1135191;
    a sio:SIO_001121 .
}

dgn-np:NP836720.RAKZDByMw7xfYwLPYD2cNZk_z-5_7sBqO_0Dz2wFr4Kgs130_provenance {
  dgn-np:NP836720.RAKZDByMw7xfYwLPYD2cNZk_z-5_7sBqO_0Dz2wFr4Kgs130_assertion dcterms:description
      "[Comparison of allele frequencies between 625 Caucasian nonaffected controls and 1,117 Caucasian individuals with systolic heart failure revealed 12 SNPs in the cardiovascular heat shock protein gene HSPB7 with greater proportional representation in the systolic heart failure group; all 12 SNPs were confirmed in an independent replication study.]. 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:20038796;
    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:NP836720.RAKZDByMw7xfYwLPYD2cNZk_z-5_7sBqO_0Dz2wFr4Kgs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:31+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" .
}