@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP205071.RARod5MGWC9Q4aH3sr3dGQKNKLdEgtbbD9-X2aBConOKg> .
@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:NP205071.RARod5MGWC9Q4aH3sr3dGQKNKLdEgtbbD9-X2aBConOKg130_head {
  this: np:hasAssertion dgn-np:NP205071.RARod5MGWC9Q4aH3sr3dGQKNKLdEgtbbD9-X2aBConOKg130_assertion;
    np:hasProvenance dgn-np:NP205071.RARod5MGWC9Q4aH3sr3dGQKNKLdEgtbbD9-X2aBConOKg130_provenance;
    np:hasPublicationInfo dgn-np:NP205071.RARod5MGWC9Q4aH3sr3dGQKNKLdEgtbbD9-X2aBConOKg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP205071.RARod5MGWC9Q4aH3sr3dGQKNKLdEgtbbD9-X2aBConOKg130_assertion a np:Assertion .
  
  dgn-np:NP205071.RARod5MGWC9Q4aH3sr3dGQKNKLdEgtbbD9-X2aBConOKg130_provenance a np:Provenance .
  
  dgn-np:NP205071.RARod5MGWC9Q4aH3sr3dGQKNKLdEgtbbD9-X2aBConOKg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP205071.RARod5MGWC9Q4aH3sr3dGQKNKLdEgtbbD9-X2aBConOKg130_assertion {
  miriam-gene:6520 a ncit:C16612 .
  
  lld:C0949658 a ncit:C7057 .
  
  dgn-gda:DGN7fdfdb699b963c27caa119ea7196155c sio:SIO_000628 miriam-gene:6520, lld:C0949658;
    a sio:SIO_001121 .
}

dgn-np:NP205071.RARod5MGWC9Q4aH3sr3dGQKNKLdEgtbbD9-X2aBConOKg130_provenance {
  dgn-np:NP205071.RARod5MGWC9Q4aH3sr3dGQKNKLdEgtbbD9-X2aBConOKg130_assertion dcterms:description
      "[Over 40 different mutations in the cardiac myosin heavy chain gene (MYH7) have been associated with familial hypertrophic cardiomyopathy (FHC), but no study has analyzed variation at this locus within the normal human population.]. 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:11549319;
    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:NP205071.RARod5MGWC9Q4aH3sr3dGQKNKLdEgtbbD9-X2aBConOKg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:53+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" .
}