@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP458518.RA9E84i6pQ_3kfDDpvAGbKGa3uHBwnedqFnLxv7mIerj0> .
@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/v3.0.0/void/> .

dgn-np:NP458518.RA9E84i6pQ_3kfDDpvAGbKGa3uHBwnedqFnLxv7mIerj0130_head {
  this: np:hasAssertion dgn-np:NP458518.RA9E84i6pQ_3kfDDpvAGbKGa3uHBwnedqFnLxv7mIerj0130_assertion;
    np:hasProvenance dgn-np:NP458518.RA9E84i6pQ_3kfDDpvAGbKGa3uHBwnedqFnLxv7mIerj0130_provenance;
    np:hasPublicationInfo dgn-np:NP458518.RA9E84i6pQ_3kfDDpvAGbKGa3uHBwnedqFnLxv7mIerj0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP458518.RA9E84i6pQ_3kfDDpvAGbKGa3uHBwnedqFnLxv7mIerj0130_assertion a np:Assertion .
  
  dgn-np:NP458518.RA9E84i6pQ_3kfDDpvAGbKGa3uHBwnedqFnLxv7mIerj0130_provenance a np:Provenance .
  
  dgn-np:NP458518.RA9E84i6pQ_3kfDDpvAGbKGa3uHBwnedqFnLxv7mIerj0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP458518.RA9E84i6pQ_3kfDDpvAGbKGa3uHBwnedqFnLxv7mIerj0130_assertion {
  miriam-gene:3133 a ncit:C16612 .
  
  lld:C0949658 a ncit:C7057 .
  
  dgn-gda:DGNc77e0338b3562d307d0fbf0d1cb687be sio:SIO_000628 miriam-gene:3133, lld:C0949658;
    a sio:SIO_001121 .
}

dgn-np:NP458518.RA9E84i6pQ_3kfDDpvAGbKGa3uHBwnedqFnLxv7mIerj0130_provenance {
  dgn-np:NP458518.RA9E84i6pQ_3kfDDpvAGbKGa3uHBwnedqFnLxv7mIerj0130_assertion dcterms:description
      "[While missense mutations in the beta cardiac myosin heavy chain (MHC) gene account for approximately half of all cases of familial hypertrophic cardiomyopathy, the molecular causes of sporadic hypertrophic cardiomyopathy are unknown.]. 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:1430197;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP458518.RA9E84i6pQ_3kfDDpvAGbKGa3uHBwnedqFnLxv7mIerj0130_publicationInfo {
  this: dcterms:created "2015-08-25T14:42:09+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}