@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP889763.RALyajHO3yfQ2s4mMvYEDjKRr4NzSGaaZpGOF21Lx8agM> .
@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:NP889763.RALyajHO3yfQ2s4mMvYEDjKRr4NzSGaaZpGOF21Lx8agM130_head {
  this: np:hasAssertion dgn-np:NP889763.RALyajHO3yfQ2s4mMvYEDjKRr4NzSGaaZpGOF21Lx8agM130_assertion;
    np:hasProvenance dgn-np:NP889763.RALyajHO3yfQ2s4mMvYEDjKRr4NzSGaaZpGOF21Lx8agM130_provenance;
    np:hasPublicationInfo dgn-np:NP889763.RALyajHO3yfQ2s4mMvYEDjKRr4NzSGaaZpGOF21Lx8agM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP889763.RALyajHO3yfQ2s4mMvYEDjKRr4NzSGaaZpGOF21Lx8agM130_assertion a np:Assertion .
  
  dgn-np:NP889763.RALyajHO3yfQ2s4mMvYEDjKRr4NzSGaaZpGOF21Lx8agM130_provenance a np:Provenance .
  
  dgn-np:NP889763.RALyajHO3yfQ2s4mMvYEDjKRr4NzSGaaZpGOF21Lx8agM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP889763.RALyajHO3yfQ2s4mMvYEDjKRr4NzSGaaZpGOF21Lx8agM130_assertion {
  miriam-gene:4625 a ncit:C16612 .
  
  lld:C0342788 a ncit:C7057 .
  
  dgn-gda:DGN8255341e9868ccea871afe3d43ce99bc sio:SIO_000628 miriam-gene:4625, lld:C0342788;
    a sio:SIO_001121 .
}

dgn-np:NP889763.RALyajHO3yfQ2s4mMvYEDjKRr4NzSGaaZpGOF21Lx8agM130_provenance {
  dgn-np:NP889763.RALyajHO3yfQ2s4mMvYEDjKRr4NzSGaaZpGOF21Lx8agM130_assertion dcterms:description
      "[Currently it is not possible to predict the phenotype in carriers of mutations in these genes, although it is widely accepted that mutations in the MYH7 gene predispose to severe HC, whereas TNNT2 mutations are frequently linked to sudden cardiac death (SCD) in spite of minimal hypertrophy.]. 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:12881443;
    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:NP889763.RALyajHO3yfQ2s4mMvYEDjKRr4NzSGaaZpGOF21Lx8agM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:07+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" .
}