@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP842464.RA2gOYN2AGWZHTGVhUwX3x7PBL8naaVzXvFw0qGaHk8os> .
@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:NP842464.RA2gOYN2AGWZHTGVhUwX3x7PBL8naaVzXvFw0qGaHk8os130_head {
  this: np:hasAssertion dgn-np:NP842464.RA2gOYN2AGWZHTGVhUwX3x7PBL8naaVzXvFw0qGaHk8os130_assertion ;
    np:hasProvenance dgn-np:NP842464.RA2gOYN2AGWZHTGVhUwX3x7PBL8naaVzXvFw0qGaHk8os130_provenance ;
    np:hasPublicationInfo dgn-np:NP842464.RA2gOYN2AGWZHTGVhUwX3x7PBL8naaVzXvFw0qGaHk8os130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP842464.RA2gOYN2AGWZHTGVhUwX3x7PBL8naaVzXvFw0qGaHk8os130_assertion a np:Assertion .
  dgn-np:NP842464.RA2gOYN2AGWZHTGVhUwX3x7PBL8naaVzXvFw0qGaHk8os130_provenance a np:Provenance .
  dgn-np:NP842464.RA2gOYN2AGWZHTGVhUwX3x7PBL8naaVzXvFw0qGaHk8os130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP842464.RA2gOYN2AGWZHTGVhUwX3x7PBL8naaVzXvFw0qGaHk8os130_assertion {
  miriam-gene:1756 a ncit:C16612 .
  lld:C0263214 a ncit:C7057 .
  dgn-gda:DGN0c7889243d961938ed2933d9f111159b sio:SIO_000628 miriam-gene:1756 , lld:C0263214 ;
    a sio:SIO_001121 .
}
dgn-np:NP842464.RA2gOYN2AGWZHTGVhUwX3x7PBL8naaVzXvFw0qGaHk8os130_provenance {
  dgn-np:NP842464.RA2gOYN2AGWZHTGVhUwX3x7PBL8naaVzXvFw0qGaHk8os130_assertion dcterms:description "[In the present study, we investigated frequency and heterozygosity of three polymorphic restriction sites and also four highly polymorphic (CA)(n) repeat microsatellites loci within hot spots region of human dystrophin gene in 60 healthy Iranian populations.]. 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:21774744 ;
    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:NP842464.RA2gOYN2AGWZHTGVhUwX3x7PBL8naaVzXvFw0qGaHk8os130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:35+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" .
}