@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP851943.RAiYoAflozzWRT298vDdmEYgonGod9lvaCbHcsQK_bi5c> .
@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:NP851943.RAiYoAflozzWRT298vDdmEYgonGod9lvaCbHcsQK_bi5c130_head {
  this: np:hasAssertion dgn-np:NP851943.RAiYoAflozzWRT298vDdmEYgonGod9lvaCbHcsQK_bi5c130_assertion;
    np:hasProvenance dgn-np:NP851943.RAiYoAflozzWRT298vDdmEYgonGod9lvaCbHcsQK_bi5c130_provenance;
    np:hasPublicationInfo dgn-np:NP851943.RAiYoAflozzWRT298vDdmEYgonGod9lvaCbHcsQK_bi5c130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP851943.RAiYoAflozzWRT298vDdmEYgonGod9lvaCbHcsQK_bi5c130_assertion a np:Assertion .
  
  dgn-np:NP851943.RAiYoAflozzWRT298vDdmEYgonGod9lvaCbHcsQK_bi5c130_provenance a np:Provenance .
  
  dgn-np:NP851943.RAiYoAflozzWRT298vDdmEYgonGod9lvaCbHcsQK_bi5c130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP851943.RAiYoAflozzWRT298vDdmEYgonGod9lvaCbHcsQK_bi5c130_assertion {
  miriam-gene:5555 a ncit:C16612 .
  
  lld:C0878544 a ncit:C7057 .
  
  dgn-gda:DGNa08c365ee38a57cba84872d3c78e9fdf sio:SIO_000628 miriam-gene:5555, lld:C0878544;
    a sio:SIO_001121 .
}

dgn-np:NP851943.RAiYoAflozzWRT298vDdmEYgonGod9lvaCbHcsQK_bi5c130_provenance {
  dgn-np:NP851943.RAiYoAflozzWRT298vDdmEYgonGod9lvaCbHcsQK_bi5c130_assertion dcterms:description
      "[More than 200 mutations in the cardiac sarcomeric proteins, including myosin heavy and light chains, actin, troponin, tropomyosin, myosin-binding protein-C, and titin/connectin, have been found to cause various types of cardiomyopathy in human since 1990, and more than 60 mutations in human cardiac troponin subunits have been identified in dilated, hypertrophic, and restrictive forms of cardiomyopathy.]. 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:15631686;
    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:NP851943.RAiYoAflozzWRT298vDdmEYgonGod9lvaCbHcsQK_bi5c130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:40+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" .
}