@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP234159.RAUys7sBOR6miXgZTCfkkR8J7Wqf2rBMHyA2nu_51cLro> .
@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:NP234159.RAUys7sBOR6miXgZTCfkkR8J7Wqf2rBMHyA2nu_51cLro130_head {
  this: np:hasAssertion dgn-np:NP234159.RAUys7sBOR6miXgZTCfkkR8J7Wqf2rBMHyA2nu_51cLro130_assertion;
    np:hasProvenance dgn-np:NP234159.RAUys7sBOR6miXgZTCfkkR8J7Wqf2rBMHyA2nu_51cLro130_provenance;
    np:hasPublicationInfo dgn-np:NP234159.RAUys7sBOR6miXgZTCfkkR8J7Wqf2rBMHyA2nu_51cLro130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP234159.RAUys7sBOR6miXgZTCfkkR8J7Wqf2rBMHyA2nu_51cLro130_assertion a np:Assertion .
  
  dgn-np:NP234159.RAUys7sBOR6miXgZTCfkkR8J7Wqf2rBMHyA2nu_51cLro130_provenance a np:Provenance .
  
  dgn-np:NP234159.RAUys7sBOR6miXgZTCfkkR8J7Wqf2rBMHyA2nu_51cLro130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP234159.RAUys7sBOR6miXgZTCfkkR8J7Wqf2rBMHyA2nu_51cLro130_assertion {
  miriam-gene:1605 a ncit:C16612 .
  
  lld:C0410174 a ncit:C7057 .
  
  dgn-gda:DGN7420829d683e2fc73fe1a3df61389445 sio:SIO_000628 miriam-gene:1605, lld:C0410174;
    a sio:SIO_001121 .
}

dgn-np:NP234159.RAUys7sBOR6miXgZTCfkkR8J7Wqf2rBMHyA2nu_51cLro130_provenance {
  dgn-np:NP234159.RAUys7sBOR6miXgZTCfkkR8J7Wqf2rBMHyA2nu_51cLro130_assertion dcterms:description
      "[Duchenne muscular dystrophy (DMD) is caused by the defect of dystrophin, and Fukuyama congenital muscular dystrophy (FCMD) is caused by an abnormal fukutin gene leading to the glycosylation defect of alpha-dystroglycan.]. 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:20199207;
    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:NP234159.RAUys7sBOR6miXgZTCfkkR8J7Wqf2rBMHyA2nu_51cLro130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:11+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" .
}