@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1297871.RAUyXQ4jAVphkdf6gsgKCM8FrAgHmkr6988k1_rhKd3fg> .
@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:NP1297871.RAUyXQ4jAVphkdf6gsgKCM8FrAgHmkr6988k1_rhKd3fg130_head {
  this: np:hasAssertion dgn-np:NP1297871.RAUyXQ4jAVphkdf6gsgKCM8FrAgHmkr6988k1_rhKd3fg130_assertion ;
    np:hasProvenance dgn-np:NP1297871.RAUyXQ4jAVphkdf6gsgKCM8FrAgHmkr6988k1_rhKd3fg130_provenance ;
    np:hasPublicationInfo dgn-np:NP1297871.RAUyXQ4jAVphkdf6gsgKCM8FrAgHmkr6988k1_rhKd3fg130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP1297871.RAUyXQ4jAVphkdf6gsgKCM8FrAgHmkr6988k1_rhKd3fg130_assertion a np:Assertion .
  dgn-np:NP1297871.RAUyXQ4jAVphkdf6gsgKCM8FrAgHmkr6988k1_rhKd3fg130_provenance a np:Provenance .
  dgn-np:NP1297871.RAUyXQ4jAVphkdf6gsgKCM8FrAgHmkr6988k1_rhKd3fg130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP1297871.RAUyXQ4jAVphkdf6gsgKCM8FrAgHmkr6988k1_rhKd3fg130_assertion {
  miriam-gene:1756 a ncit:C16612 .
  lld:C0026850 a ncit:C7057 .
  dgn-gda:DGNd274a2454c1e5423052d826fb70ddb97 sio:SIO_000628 miriam-gene:1756 , lld:C0026850 ;
    a sio:SIO_001121 .
}
dgn-np:NP1297871.RAUyXQ4jAVphkdf6gsgKCM8FrAgHmkr6988k1_rhKd3fg130_provenance {
  dgn-np:NP1297871.RAUyXQ4jAVphkdf6gsgKCM8FrAgHmkr6988k1_rhKd3fg130_assertion dcterms:description "[The segregation of DMD and the DXS164 deletion in this family illustrates the importance of extended pedigree analysis when DXS164 deletions are used to identify female carriers of the DMD gene.]. 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:2887110 ;
    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:NP1297871.RAUyXQ4jAVphkdf6gsgKCM8FrAgHmkr6988k1_rhKd3fg130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:34+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" .
}