@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP897490.RA9M1D-ilwXmbrTPPT431EwpCKotQ7WHZIQ0sS0647SgM> .
@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:NP897490.RA9M1D-ilwXmbrTPPT431EwpCKotQ7WHZIQ0sS0647SgM130_head {
  this: np:hasAssertion dgn-np:NP897490.RA9M1D-ilwXmbrTPPT431EwpCKotQ7WHZIQ0sS0647SgM130_assertion;
    np:hasProvenance dgn-np:NP897490.RA9M1D-ilwXmbrTPPT431EwpCKotQ7WHZIQ0sS0647SgM130_provenance;
    np:hasPublicationInfo dgn-np:NP897490.RA9M1D-ilwXmbrTPPT431EwpCKotQ7WHZIQ0sS0647SgM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP897490.RA9M1D-ilwXmbrTPPT431EwpCKotQ7WHZIQ0sS0647SgM130_assertion a np:Assertion .
  
  dgn-np:NP897490.RA9M1D-ilwXmbrTPPT431EwpCKotQ7WHZIQ0sS0647SgM130_provenance a np:Provenance .
  
  dgn-np:NP897490.RA9M1D-ilwXmbrTPPT431EwpCKotQ7WHZIQ0sS0647SgM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP897490.RA9M1D-ilwXmbrTPPT431EwpCKotQ7WHZIQ0sS0647SgM130_assertion {
  miriam-gene:6046 a ncit:C16612 .
  
  lld:C0026848 a ncit:C7057 .
  
  dgn-gda:DGN5fdac2a8157ac763cea670dadaeb5c17 sio:SIO_000628 miriam-gene:6046, lld:C0026848;
    a sio:SIO_001121 .
}

dgn-np:NP897490.RA9M1D-ilwXmbrTPPT431EwpCKotQ7WHZIQ0sS0647SgM130_provenance {
  dgn-np:NP897490.RA9M1D-ilwXmbrTPPT431EwpCKotQ7WHZIQ0sS0647SgM130_assertion dcterms:description
      "[Serum creatine-kinase (CK) isoenzyme MB was measured in 53 patients affected by different types of myopathies (20 with Duchenne muscular dystrophy (DMD), eight with the Becker form (BMD), ten with the limb-girdle form (LGMD), six with the facioscapulohumeral form (FSH), and nine affected by polymyositis and in 21 normal control subjects).]. 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:4050853;
    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:NP897490.RA9M1D-ilwXmbrTPPT431EwpCKotQ7WHZIQ0sS0647SgM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:11+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" .
}