@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP539926.RABle0BO7oSLjVUMnBjIXLNr0cHDKz6ihxlHlz_YPmflY> .
@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:NP539926.RABle0BO7oSLjVUMnBjIXLNr0cHDKz6ihxlHlz_YPmflY130_head {
  this: np:hasAssertion dgn-np:NP539926.RABle0BO7oSLjVUMnBjIXLNr0cHDKz6ihxlHlz_YPmflY130_assertion;
    np:hasProvenance dgn-np:NP539926.RABle0BO7oSLjVUMnBjIXLNr0cHDKz6ihxlHlz_YPmflY130_provenance;
    np:hasPublicationInfo dgn-np:NP539926.RABle0BO7oSLjVUMnBjIXLNr0cHDKz6ihxlHlz_YPmflY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP539926.RABle0BO7oSLjVUMnBjIXLNr0cHDKz6ihxlHlz_YPmflY130_assertion a np:Assertion .
  
  dgn-np:NP539926.RABle0BO7oSLjVUMnBjIXLNr0cHDKz6ihxlHlz_YPmflY130_provenance a np:Provenance .
  
  dgn-np:NP539926.RABle0BO7oSLjVUMnBjIXLNr0cHDKz6ihxlHlz_YPmflY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP539926.RABle0BO7oSLjVUMnBjIXLNr0cHDKz6ihxlHlz_YPmflY130_assertion {
  miriam-gene:84665 a ncit:C16612 .
  
  lld:C1449563 a ncit:C7057 .
  
  dgn-gda:DGN5376f9d29ba63c61ac67df20eb78b307 sio:SIO_000628 miriam-gene:84665, lld:C1449563;
    a sio:SIO_001121 .
}

dgn-np:NP539926.RABle0BO7oSLjVUMnBjIXLNr0cHDKz6ihxlHlz_YPmflY130_provenance {
  dgn-np:NP539926.RABle0BO7oSLjVUMnBjIXLNr0cHDKz6ihxlHlz_YPmflY130_assertion dcterms:description
      "[According to our epidemiological data, the prevalence of ANKRD1 mutations seems to be lower than that of its binding partner myopalladin, indicating the clinical significance of myopalladin for the functional integrity of the sarcomeric apparatus and the protection against DCM.]. 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:22892539;
    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:NP539926.RABle0BO7oSLjVUMnBjIXLNr0cHDKz6ihxlHlz_YPmflY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:25+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" .
}