@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP64262.RA_3pMJ-c9cuj8MQUB1iAAxobXWj9vJ9i6CWogTNMV-64> .
@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:NP64262.RA_3pMJ-c9cuj8MQUB1iAAxobXWj9vJ9i6CWogTNMV-64130_head {
  this: np:hasAssertion dgn-np:NP64262.RA_3pMJ-c9cuj8MQUB1iAAxobXWj9vJ9i6CWogTNMV-64130_assertion;
    np:hasProvenance dgn-np:NP64262.RA_3pMJ-c9cuj8MQUB1iAAxobXWj9vJ9i6CWogTNMV-64130_provenance;
    np:hasPublicationInfo dgn-np:NP64262.RA_3pMJ-c9cuj8MQUB1iAAxobXWj9vJ9i6CWogTNMV-64130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP64262.RA_3pMJ-c9cuj8MQUB1iAAxobXWj9vJ9i6CWogTNMV-64130_assertion a np:Assertion .
  
  dgn-np:NP64262.RA_3pMJ-c9cuj8MQUB1iAAxobXWj9vJ9i6CWogTNMV-64130_provenance a np:Provenance .
  
  dgn-np:NP64262.RA_3pMJ-c9cuj8MQUB1iAAxobXWj9vJ9i6CWogTNMV-64130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP64262.RA_3pMJ-c9cuj8MQUB1iAAxobXWj9vJ9i6CWogTNMV-64130_assertion {
  miriam-gene:1674 a ncit:C16612 .
  
  lld:C0878544 a ncit:C7057 .
  
  dgn-gda:DGN29d09458862d77a4224b65dbeda75fe3 sio:SIO_000628 miriam-gene:1674, lld:C0878544;
    a sio:SIO_001122 .
}

dgn-np:NP64262.RA_3pMJ-c9cuj8MQUB1iAAxobXWj9vJ9i6CWogTNMV-64130_provenance {
  dgn-np:NP64262.RA_3pMJ-c9cuj8MQUB1iAAxobXWj9vJ9i6CWogTNMV-64130_assertion dcterms:description
      "[The lack of severe disruption of cytoskeletal desmin network formation seen with mutations in the 1A and tail domains suggests that dysfunction of seemingly intact desmin networks is sufficient to cause DCM.]. 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:17325244;
    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:NP64262.RA_3pMJ-c9cuj8MQUB1iAAxobXWj9vJ9i6CWogTNMV-64130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:30+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" .
}