@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP808146.RAJYbR8eoHam0PAjqXFLj9Vh6Gn-2aet5-hhno3e7oG_0> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP808146.RAJYbR8eoHam0PAjqXFLj9Vh6Gn-2aet5-hhno3e7oG_0130_head {
  this: np:hasAssertion dgn-np:NP808146.RAJYbR8eoHam0PAjqXFLj9Vh6Gn-2aet5-hhno3e7oG_0130_assertion;
    np:hasProvenance dgn-np:NP808146.RAJYbR8eoHam0PAjqXFLj9Vh6Gn-2aet5-hhno3e7oG_0130_provenance;
    np:hasPublicationInfo dgn-np:NP808146.RAJYbR8eoHam0PAjqXFLj9Vh6Gn-2aet5-hhno3e7oG_0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP808146.RAJYbR8eoHam0PAjqXFLj9Vh6Gn-2aet5-hhno3e7oG_0130_assertion a np:Assertion .
  
  dgn-np:NP808146.RAJYbR8eoHam0PAjqXFLj9Vh6Gn-2aet5-hhno3e7oG_0130_provenance a np:Provenance .
  
  dgn-np:NP808146.RAJYbR8eoHam0PAjqXFLj9Vh6Gn-2aet5-hhno3e7oG_0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP808146.RAJYbR8eoHam0PAjqXFLj9Vh6Gn-2aet5-hhno3e7oG_0130_assertion {
  miriam-gene:6520 a ncit:C16612 .
  
  lld:C1533847 a ncit:C7057 .
  
  dgn-gda:DGN0ae718cc0b977357cc93326200360f70 sio:SIO_000628 miriam-gene:6520, lld:C1533847;
    a sio:SIO_001122 .
}

dgn-np:NP808146.RAJYbR8eoHam0PAjqXFLj9Vh6Gn-2aet5-hhno3e7oG_0130_provenance {
  dgn-np:NP808146.RAJYbR8eoHam0PAjqXFLj9Vh6Gn-2aet5-hhno3e7oG_0130_assertion dcterms:description
      "[Heterozygous dominant missense mutations in myosin heavy chain genes cause various types of cardiomyopathy and skeletal myopathy, but the effects of myosin heavy chain null mutations in humans have not previously been reported.]. 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:20418530;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP808146.RAJYbR8eoHam0PAjqXFLj9Vh6Gn-2aet5-hhno3e7oG_0130_publicationInfo {
  this: dcterms:created "2016-05-13T12:47:51+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}