@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP469666.RAuwevyAUloEj9iQ1YT5CuhGazJ3OFaTbTrHNHqEK6zbM> .
@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:NP469666.RAuwevyAUloEj9iQ1YT5CuhGazJ3OFaTbTrHNHqEK6zbM130_head {
  this: np:hasAssertion dgn-np:NP469666.RAuwevyAUloEj9iQ1YT5CuhGazJ3OFaTbTrHNHqEK6zbM130_assertion ;
    np:hasProvenance dgn-np:NP469666.RAuwevyAUloEj9iQ1YT5CuhGazJ3OFaTbTrHNHqEK6zbM130_provenance ;
    np:hasPublicationInfo dgn-np:NP469666.RAuwevyAUloEj9iQ1YT5CuhGazJ3OFaTbTrHNHqEK6zbM130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP469666.RAuwevyAUloEj9iQ1YT5CuhGazJ3OFaTbTrHNHqEK6zbM130_provenance a np:Provenance .
  dgn-np:NP469666.RAuwevyAUloEj9iQ1YT5CuhGazJ3OFaTbTrHNHqEK6zbM130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP469666.RAuwevyAUloEj9iQ1YT5CuhGazJ3OFaTbTrHNHqEK6zbM130_assertion {
  miriam-gene:7273 a ncit:C16612 .
  lld:C0007193 a ncit:C7057 .
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}
dgn-np:NP469666.RAuwevyAUloEj9iQ1YT5CuhGazJ3OFaTbTrHNHqEK6zbM130_provenance {
  dgn-np:NP469666.RAuwevyAUloEj9iQ1YT5CuhGazJ3OFaTbTrHNHqEK6zbM130_assertion dcterms:description "[Incorporation of sequencing approaches that detect TTN truncations into genetic testing for dilated cardiomyopathy should substantially increase test sensitivity, thereby allowing earlier diagnosis and therapeutic intervention for many patients with dilated cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
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    sio:SIO_000772 miriam-pubmed:22335739 ;
    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:NP469666.RAuwevyAUloEj9iQ1YT5CuhGazJ3OFaTbTrHNHqEK6zbM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:41+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
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