@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP58820.RAnT7-c3poLQvux1t6Lch1EiAfWrnnLm03TN_q0q0GeyM> .
@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:NP58820.RAnT7-c3poLQvux1t6Lch1EiAfWrnnLm03TN_q0q0GeyM130_head {
  this: np:hasAssertion dgn-np:NP58820.RAnT7-c3poLQvux1t6Lch1EiAfWrnnLm03TN_q0q0GeyM130_assertion;
    np:hasProvenance dgn-np:NP58820.RAnT7-c3poLQvux1t6Lch1EiAfWrnnLm03TN_q0q0GeyM130_provenance;
    np:hasPublicationInfo dgn-np:NP58820.RAnT7-c3poLQvux1t6Lch1EiAfWrnnLm03TN_q0q0GeyM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP58820.RAnT7-c3poLQvux1t6Lch1EiAfWrnnLm03TN_q0q0GeyM130_assertion a np:Assertion .
  
  dgn-np:NP58820.RAnT7-c3poLQvux1t6Lch1EiAfWrnnLm03TN_q0q0GeyM130_provenance a np:Provenance .
  
  dgn-np:NP58820.RAnT7-c3poLQvux1t6Lch1EiAfWrnnLm03TN_q0q0GeyM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP58820.RAnT7-c3poLQvux1t6Lch1EiAfWrnnLm03TN_q0q0GeyM130_assertion {
  miriam-gene:7168 a ncit:C16612 .
  
  lld:C0007194 a ncit:C7057 .
  
  dgn-gda:DGN77f07e99054b0bdb26c8401d7213971a sio:SIO_000628 miriam-gene:7168, lld:C0007194;
    a sio:SIO_001122 .
}

dgn-np:NP58820.RAnT7-c3poLQvux1t6Lch1EiAfWrnnLm03TN_q0q0GeyM130_provenance {
  dgn-np:NP58820.RAnT7-c3poLQvux1t6Lch1EiAfWrnnLm03TN_q0q0GeyM130_assertion dcterms:description
      "[ Mutations in genes encoding thin filament proteins are less prevalent in HCM than previously estimated. Patients with mutations in troponin T, troponin I, alpha-tropomyosin, and actin do not invariably present with any distinct clinical feature, thus limiting the utility of gene status for risk stratification or of clinical phenotype in guiding individual genetic screening at this time.]. 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:12860912;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP58820.RAnT7-c3poLQvux1t6Lch1EiAfWrnnLm03TN_q0q0GeyM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:27+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" .
}