@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP268440.RAXwupwhSQkwgkyiZpNo69EGCq7tHMZWoZTbSDtA6zCRA> .
@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:NP268440.RAXwupwhSQkwgkyiZpNo69EGCq7tHMZWoZTbSDtA6zCRA130_head {
  this: np:hasAssertion dgn-np:NP268440.RAXwupwhSQkwgkyiZpNo69EGCq7tHMZWoZTbSDtA6zCRA130_assertion;
    np:hasProvenance dgn-np:NP268440.RAXwupwhSQkwgkyiZpNo69EGCq7tHMZWoZTbSDtA6zCRA130_provenance;
    np:hasPublicationInfo dgn-np:NP268440.RAXwupwhSQkwgkyiZpNo69EGCq7tHMZWoZTbSDtA6zCRA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP268440.RAXwupwhSQkwgkyiZpNo69EGCq7tHMZWoZTbSDtA6zCRA130_assertion a np:Assertion .
  
  dgn-np:NP268440.RAXwupwhSQkwgkyiZpNo69EGCq7tHMZWoZTbSDtA6zCRA130_provenance a np:Provenance .
  
  dgn-np:NP268440.RAXwupwhSQkwgkyiZpNo69EGCq7tHMZWoZTbSDtA6zCRA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP268440.RAXwupwhSQkwgkyiZpNo69EGCq7tHMZWoZTbSDtA6zCRA130_assertion {
  miriam-gene:6588 a ncit:C16612 .
  
  lld:C0039685 a ncit:C7057 .
  
  dgn-gda:DGN595d8bb831ab7d439f4d12024c0d0aa9 sio:SIO_000628 miriam-gene:6588, lld:C0039685;
    a sio:SIO_001121 .
}

dgn-np:NP268440.RAXwupwhSQkwgkyiZpNo69EGCq7tHMZWoZTbSDtA6zCRA130_provenance {
  dgn-np:NP268440.RAXwupwhSQkwgkyiZpNo69EGCq7tHMZWoZTbSDtA6zCRA130_assertion dcterms:description
      "[Our objective was to evaluate SERCA2a (i.e., the SERCA cardiac isoform), PLN, SLN, and RyR2 (i.e., the RyR isoform enriched in the heart) gene expression in myocardial tissue of patients affected by tetralogy of Fallot (TOF), a conotruncal heart defect.]. 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:17515962;
    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:NP268440.RAXwupwhSQkwgkyiZpNo69EGCq7tHMZWoZTbSDtA6zCRA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:30+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" .
}