@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP708904.RAGEICImYApsowAw1pyXDYJui3Y_U6TfDBPK2E9zneBoI> .
@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:NP708904.RAGEICImYApsowAw1pyXDYJui3Y_U6TfDBPK2E9zneBoI130_head {
  this: np:hasAssertion dgn-np:NP708904.RAGEICImYApsowAw1pyXDYJui3Y_U6TfDBPK2E9zneBoI130_assertion;
    np:hasProvenance dgn-np:NP708904.RAGEICImYApsowAw1pyXDYJui3Y_U6TfDBPK2E9zneBoI130_provenance;
    np:hasPublicationInfo dgn-np:NP708904.RAGEICImYApsowAw1pyXDYJui3Y_U6TfDBPK2E9zneBoI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP708904.RAGEICImYApsowAw1pyXDYJui3Y_U6TfDBPK2E9zneBoI130_assertion a np:Assertion .
  
  dgn-np:NP708904.RAGEICImYApsowAw1pyXDYJui3Y_U6TfDBPK2E9zneBoI130_provenance a np:Provenance .
  
  dgn-np:NP708904.RAGEICImYApsowAw1pyXDYJui3Y_U6TfDBPK2E9zneBoI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP708904.RAGEICImYApsowAw1pyXDYJui3Y_U6TfDBPK2E9zneBoI130_assertion {
  miriam-gene:7402 a ncit:C16612 .
  
  lld:C0022821 a ncit:C7057 .
  
  dgn-gda:DGN89fe82a5f9333b3e8ae9f432268f7c0d sio:SIO_000628 miriam-gene:7402, lld:C0022821;
    a sio:SIO_001121 .
}

dgn-np:NP708904.RAGEICImYApsowAw1pyXDYJui3Y_U6TfDBPK2E9zneBoI130_provenance {
  dgn-np:NP708904.RAGEICImYApsowAw1pyXDYJui3Y_U6TfDBPK2E9zneBoI130_assertion dcterms:description
      "[These mice show many pathologic and phenotypic signs typical of DMD in humans including kyphosis and shorter life span, all of which are not seen in the mdx mice due to their utrophin upregulation that partially compensates the loss of dystrophin functions and leads to mild phenotypes.]. 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:18973234;
    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:NP708904.RAGEICImYApsowAw1pyXDYJui3Y_U6TfDBPK2E9zneBoI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:10+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" .
}