@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP797490.RASWSjHcNbnLlePHWiGPBQcmk30pfYeJXAILwGvyPs204> .
@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:NP797490.RASWSjHcNbnLlePHWiGPBQcmk30pfYeJXAILwGvyPs204130_head {
  this: np:hasAssertion dgn-np:NP797490.RASWSjHcNbnLlePHWiGPBQcmk30pfYeJXAILwGvyPs204130_assertion;
    np:hasProvenance dgn-np:NP797490.RASWSjHcNbnLlePHWiGPBQcmk30pfYeJXAILwGvyPs204130_provenance;
    np:hasPublicationInfo dgn-np:NP797490.RASWSjHcNbnLlePHWiGPBQcmk30pfYeJXAILwGvyPs204130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP797490.RASWSjHcNbnLlePHWiGPBQcmk30pfYeJXAILwGvyPs204130_assertion a np:Assertion .
  
  dgn-np:NP797490.RASWSjHcNbnLlePHWiGPBQcmk30pfYeJXAILwGvyPs204130_provenance a np:Provenance .
  
  dgn-np:NP797490.RASWSjHcNbnLlePHWiGPBQcmk30pfYeJXAILwGvyPs204130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP797490.RASWSjHcNbnLlePHWiGPBQcmk30pfYeJXAILwGvyPs204130_assertion {
  miriam-gene:1756 a ncit:C16612 .
  
  lld:C0013264 a ncit:C7057 .
  
  dgn-gda:DGNff5e101cff163670d9dd0c67bc96793e sio:SIO_000628 miriam-gene:1756, lld:C0013264;
    a sio:SIO_001121 .
}

dgn-np:NP797490.RASWSjHcNbnLlePHWiGPBQcmk30pfYeJXAILwGvyPs204130_provenance {
  dgn-np:NP797490.RASWSjHcNbnLlePHWiGPBQcmk30pfYeJXAILwGvyPs204130_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-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:NP797490.RASWSjHcNbnLlePHWiGPBQcmk30pfYeJXAILwGvyPs204130_publicationInfo {
  this: dcterms:created "2016-05-13T12:47:46+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" .
}