@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP184390.RAUzEEJMc_m5PvDGrtxugRxbc_X2CrmsPu7g4JS5vdkso> .
@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:NP184390.RAUzEEJMc_m5PvDGrtxugRxbc_X2CrmsPu7g4JS5vdkso130_head {
  this: np:hasAssertion dgn-np:NP184390.RAUzEEJMc_m5PvDGrtxugRxbc_X2CrmsPu7g4JS5vdkso130_assertion;
    np:hasProvenance dgn-np:NP184390.RAUzEEJMc_m5PvDGrtxugRxbc_X2CrmsPu7g4JS5vdkso130_provenance;
    np:hasPublicationInfo dgn-np:NP184390.RAUzEEJMc_m5PvDGrtxugRxbc_X2CrmsPu7g4JS5vdkso130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP184390.RAUzEEJMc_m5PvDGrtxugRxbc_X2CrmsPu7g4JS5vdkso130_assertion a np:Assertion .
  
  dgn-np:NP184390.RAUzEEJMc_m5PvDGrtxugRxbc_X2CrmsPu7g4JS5vdkso130_provenance a np:Provenance .
  
  dgn-np:NP184390.RAUzEEJMc_m5PvDGrtxugRxbc_X2CrmsPu7g4JS5vdkso130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP184390.RAUzEEJMc_m5PvDGrtxugRxbc_X2CrmsPu7g4JS5vdkso130_assertion {
  miriam-gene:1756 a ncit:C16612 .
  
  lld:C0339510 a ncit:C7057 .
  
  dgn-gda:DGN2454eabaa3685be58cb281a28707cdea sio:SIO_000628 miriam-gene:1756, lld:C0339510;
    a sio:SIO_001121 .
}

dgn-np:NP184390.RAUzEEJMc_m5PvDGrtxugRxbc_X2CrmsPu7g4JS5vdkso130_provenance {
  dgn-np:NP184390.RAUzEEJMc_m5PvDGrtxugRxbc_X2CrmsPu7g4JS5vdkso130_assertion dcterms:description
      "[Estimating carrier risks for female relatives of Duchenne (DMD) and Becker (BMD) dystrophy sufferers depends upon calculation of segregational risks, supplemented by enzyme tests which show considerable overlap between carrier and control data.]. 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:2688825;
    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:NP184390.RAUzEEJMc_m5PvDGrtxugRxbc_X2CrmsPu7g4JS5vdkso130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:39+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" .
}