@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP530432.RAVifLvSf33ehBzdAlY3EMOttD-sGqWesaW7wnyGZE9Uw> .
@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:NP530432.RAVifLvSf33ehBzdAlY3EMOttD-sGqWesaW7wnyGZE9Uw130_head {
  this: np:hasAssertion dgn-np:NP530432.RAVifLvSf33ehBzdAlY3EMOttD-sGqWesaW7wnyGZE9Uw130_assertion;
    np:hasProvenance dgn-np:NP530432.RAVifLvSf33ehBzdAlY3EMOttD-sGqWesaW7wnyGZE9Uw130_provenance;
    np:hasPublicationInfo dgn-np:NP530432.RAVifLvSf33ehBzdAlY3EMOttD-sGqWesaW7wnyGZE9Uw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP530432.RAVifLvSf33ehBzdAlY3EMOttD-sGqWesaW7wnyGZE9Uw130_assertion a np:Assertion .
  
  dgn-np:NP530432.RAVifLvSf33ehBzdAlY3EMOttD-sGqWesaW7wnyGZE9Uw130_provenance a np:Provenance .
  
  dgn-np:NP530432.RAVifLvSf33ehBzdAlY3EMOttD-sGqWesaW7wnyGZE9Uw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP530432.RAVifLvSf33ehBzdAlY3EMOttD-sGqWesaW7wnyGZE9Uw130_assertion {
  miriam-gene:1756 a ncit:C16612 .
  
  lld:C0410174 a ncit:C7057 .
  
  dgn-gda:DGN40b75cd95cde49fe26d59573cb4495a8 sio:SIO_000628 miriam-gene:1756, lld:C0410174;
    a sio:SIO_001121 .
}

dgn-np:NP530432.RAVifLvSf33ehBzdAlY3EMOttD-sGqWesaW7wnyGZE9Uw130_provenance {
  dgn-np:NP530432.RAVifLvSf33ehBzdAlY3EMOttD-sGqWesaW7wnyGZE9Uw130_assertion dcterms:description
      "[Although DNA analysis by Southern blotting with complementary DNAs representing the whole of the dystrophin coding sequence detected neither gross deletions nor duplications, immunohistochemistry and Western blotting of the biopsied skeletal muscle with an antidystrophin monoclonal antibody (dystrophin test) showed that the approximately 400-kd dystrophin was expressed normally at the sarcoplasmic membrane of the FCMD phenotype patient but was completely absent in the DMD phenotype patient.]. 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:1875028;
    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:NP530432.RAVifLvSf33ehBzdAlY3EMOttD-sGqWesaW7wnyGZE9Uw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:20+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" .
}