@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1295593.RA7Wh8PE4FgRu80-7wMp69QD7Rd42odMW6exfTat3v5gE> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP1295593.RA7Wh8PE4FgRu80-7wMp69QD7Rd42odMW6exfTat3v5gE130_head {
  this: np:hasAssertion dgn-np:NP1295593.RA7Wh8PE4FgRu80-7wMp69QD7Rd42odMW6exfTat3v5gE130_assertion;
    np:hasProvenance dgn-np:NP1295593.RA7Wh8PE4FgRu80-7wMp69QD7Rd42odMW6exfTat3v5gE130_provenance;
    np:hasPublicationInfo dgn-np:NP1295593.RA7Wh8PE4FgRu80-7wMp69QD7Rd42odMW6exfTat3v5gE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1295593.RA7Wh8PE4FgRu80-7wMp69QD7Rd42odMW6exfTat3v5gE130_assertion a np:Assertion .
  
  dgn-np:NP1295593.RA7Wh8PE4FgRu80-7wMp69QD7Rd42odMW6exfTat3v5gE130_provenance a np:Provenance .
  
  dgn-np:NP1295593.RA7Wh8PE4FgRu80-7wMp69QD7Rd42odMW6exfTat3v5gE130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1295593.RA7Wh8PE4FgRu80-7wMp69QD7Rd42odMW6exfTat3v5gE130_assertion {
  miriam-gene:1756 a ncit:C16612 .
  
  lld:C0026850 a ncit:C7057 .
  
  dgn-gda:DGNe3141115469118561169f18db9a70952 sio:SIO_000628 miriam-gene:1756, lld:C0026850;
    a sio:SIO_001121 .
}

dgn-np:NP1295593.RA7Wh8PE4FgRu80-7wMp69QD7Rd42odMW6exfTat3v5gE130_provenance {
  dgn-np:NP1295593.RA7Wh8PE4FgRu80-7wMp69QD7Rd42odMW6exfTat3v5gE130_assertion dcterms:description
      "[Somatic cell testing of dystrophin expression may offer an alternative to established genetic carrier tests for those women in whom deletions of the DMD are not detectable, whose pedigree structure does not permit linkage analysis, or in whom standard phenotypic analyses are ambiguous.]. 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:2658563;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1295593.RA7Wh8PE4FgRu80-7wMp69QD7Rd42odMW6exfTat3v5gE130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:33+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}