@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP216087.RAO2UFquFuyBSoS5cQ-JXqMqE4G1M3Ufz9vAzWjwuDVv8> .
@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:NP216087.RAO2UFquFuyBSoS5cQ-JXqMqE4G1M3Ufz9vAzWjwuDVv8130_head {
  this: np:hasAssertion dgn-np:NP216087.RAO2UFquFuyBSoS5cQ-JXqMqE4G1M3Ufz9vAzWjwuDVv8130_assertion;
    np:hasProvenance dgn-np:NP216087.RAO2UFquFuyBSoS5cQ-JXqMqE4G1M3Ufz9vAzWjwuDVv8130_provenance;
    np:hasPublicationInfo dgn-np:NP216087.RAO2UFquFuyBSoS5cQ-JXqMqE4G1M3Ufz9vAzWjwuDVv8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP216087.RAO2UFquFuyBSoS5cQ-JXqMqE4G1M3Ufz9vAzWjwuDVv8130_assertion a np:Assertion .
  
  dgn-np:NP216087.RAO2UFquFuyBSoS5cQ-JXqMqE4G1M3Ufz9vAzWjwuDVv8130_provenance a np:Provenance .
  
  dgn-np:NP216087.RAO2UFquFuyBSoS5cQ-JXqMqE4G1M3Ufz9vAzWjwuDVv8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP216087.RAO2UFquFuyBSoS5cQ-JXqMqE4G1M3Ufz9vAzWjwuDVv8130_assertion {
  miriam-gene:183 a ncit:C16612 .
  
  lld:C0018802 a ncit:C7057 .
  
  dgn-gda:DGNf100621f236986bd1d99ed69b64ea866 sio:SIO_000628 miriam-gene:183, lld:C0018802;
    a sio:SIO_001121 .
}

dgn-np:NP216087.RAO2UFquFuyBSoS5cQ-JXqMqE4G1M3Ufz9vAzWjwuDVv8130_provenance {
  dgn-np:NP216087.RAO2UFquFuyBSoS5cQ-JXqMqE4G1M3Ufz9vAzWjwuDVv8130_assertion dcterms:description
      "[Our results show that angiotensin II and hypoxia, signals common to HF, result in increased LUC7L3 and RBM25 splicing regulators, increased binding of RBM25 to SCN5A mRNA, increased SCN5A splice variant abundances, decreased full-length SCN5A mRNA and protein, and decreased Na(+) current.]. 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:22939879;
    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:NP216087.RAO2UFquFuyBSoS5cQ-JXqMqE4G1M3Ufz9vAzWjwuDVv8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:00+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" .
}