@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP277427.RAUNLpFYYqqHRsSCltEvl26BTA9mxRPccTfD1bPm6cmpI> .
@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:NP277427.RAUNLpFYYqqHRsSCltEvl26BTA9mxRPccTfD1bPm6cmpI130_head {
  this: np:hasAssertion dgn-np:NP277427.RAUNLpFYYqqHRsSCltEvl26BTA9mxRPccTfD1bPm6cmpI130_assertion;
    np:hasProvenance dgn-np:NP277427.RAUNLpFYYqqHRsSCltEvl26BTA9mxRPccTfD1bPm6cmpI130_provenance;
    np:hasPublicationInfo dgn-np:NP277427.RAUNLpFYYqqHRsSCltEvl26BTA9mxRPccTfD1bPm6cmpI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP277427.RAUNLpFYYqqHRsSCltEvl26BTA9mxRPccTfD1bPm6cmpI130_assertion a np:Assertion .
  
  dgn-np:NP277427.RAUNLpFYYqqHRsSCltEvl26BTA9mxRPccTfD1bPm6cmpI130_provenance a np:Provenance .
  
  dgn-np:NP277427.RAUNLpFYYqqHRsSCltEvl26BTA9mxRPccTfD1bPm6cmpI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP277427.RAUNLpFYYqqHRsSCltEvl26BTA9mxRPccTfD1bPm6cmpI130_assertion {
  miriam-gene:5554 a ncit:C16612 .
  
  lld:C1449563 a ncit:C7057 .
  
  dgn-gda:DGN4a40cd1a7d225e6719d7248e78c9f77c sio:SIO_000628 miriam-gene:5554, lld:C1449563;
    a sio:SIO_001121 .
}

dgn-np:NP277427.RAUNLpFYYqqHRsSCltEvl26BTA9mxRPccTfD1bPm6cmpI130_provenance {
  dgn-np:NP277427.RAUNLpFYYqqHRsSCltEvl26BTA9mxRPccTfD1bPm6cmpI130_assertion dcterms:description
      "[While mutations in different myosin binding protein C (MYBPC) genes are well known causes of various human diseases, such as hypertrophic (HCM) and dilated (DCM) forms of cardiomyopathy as well as skeletal muscular disorders, the underlying molecular mechanisms remain not well understood.]. 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:22173300;
    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:NP277427.RAUNLpFYYqqHRsSCltEvl26BTA9mxRPccTfD1bPm6cmpI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:36+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" .
}