@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP185486.RABkqycfP3sU2TIHyUKUtPQU4Vaad4vTLm0jiGFQPs8mU> .
@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:NP185486.RABkqycfP3sU2TIHyUKUtPQU4Vaad4vTLm0jiGFQPs8mU130_head {
  this: np:hasAssertion dgn-np:NP185486.RABkqycfP3sU2TIHyUKUtPQU4Vaad4vTLm0jiGFQPs8mU130_assertion;
    np:hasProvenance dgn-np:NP185486.RABkqycfP3sU2TIHyUKUtPQU4Vaad4vTLm0jiGFQPs8mU130_provenance;
    np:hasPublicationInfo dgn-np:NP185486.RABkqycfP3sU2TIHyUKUtPQU4Vaad4vTLm0jiGFQPs8mU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP185486.RABkqycfP3sU2TIHyUKUtPQU4Vaad4vTLm0jiGFQPs8mU130_assertion a np:Assertion .
  
  dgn-np:NP185486.RABkqycfP3sU2TIHyUKUtPQU4Vaad4vTLm0jiGFQPs8mU130_provenance a np:Provenance .
  
  dgn-np:NP185486.RABkqycfP3sU2TIHyUKUtPQU4Vaad4vTLm0jiGFQPs8mU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP185486.RABkqycfP3sU2TIHyUKUtPQU4Vaad4vTLm0jiGFQPs8mU130_assertion {
  miriam-gene:8170 a ncit:C16612 .
  
  lld:C0007194 a ncit:C7057 .
  
  dgn-gda:DGNf90569e478873277b28259d0b83d8318 sio:SIO_000628 miriam-gene:8170, lld:C0007194;
    a sio:SIO_001121 .
}

dgn-np:NP185486.RABkqycfP3sU2TIHyUKUtPQU4Vaad4vTLm0jiGFQPs8mU130_provenance {
  dgn-np:NP185486.RABkqycfP3sU2TIHyUKUtPQU4Vaad4vTLm0jiGFQPs8mU130_assertion dcterms:description
      "[In conclusion, our data suggest that 15 bp-deletion and C-insertion in the 5'UTR region of MEF2C could affect hypertrophic cardiomyopathy, potentially by affecting expression of MEF2C and therefore, the expression of their target cardiac proteins that are implicated in the hypertrophic process.]. 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:22718505;
    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:NP185486.RABkqycfP3sU2TIHyUKUtPQU4Vaad4vTLm0jiGFQPs8mU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:42+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" .
}