@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP350428.RA1iizsrBGXyWLW_rQID7OhmvnvET_oopXBP5WYsSwpn4> .
@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:NP350428.RA1iizsrBGXyWLW_rQID7OhmvnvET_oopXBP5WYsSwpn4130_head {
  this: np:hasAssertion dgn-np:NP350428.RA1iizsrBGXyWLW_rQID7OhmvnvET_oopXBP5WYsSwpn4130_assertion ;
    np:hasProvenance dgn-np:NP350428.RA1iizsrBGXyWLW_rQID7OhmvnvET_oopXBP5WYsSwpn4130_provenance ;
    np:hasPublicationInfo dgn-np:NP350428.RA1iizsrBGXyWLW_rQID7OhmvnvET_oopXBP5WYsSwpn4130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP350428.RA1iizsrBGXyWLW_rQID7OhmvnvET_oopXBP5WYsSwpn4130_assertion a np:Assertion .
  dgn-np:NP350428.RA1iizsrBGXyWLW_rQID7OhmvnvET_oopXBP5WYsSwpn4130_provenance a np:Provenance .
  dgn-np:NP350428.RA1iizsrBGXyWLW_rQID7OhmvnvET_oopXBP5WYsSwpn4130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP350428.RA1iizsrBGXyWLW_rQID7OhmvnvET_oopXBP5WYsSwpn4130_assertion {
  miriam-gene:25759 a ncit:C16612 .
  lld:C0013264 a ncit:C7057 .
  dgn-gda:DGNb48ab9126a4e4cb29d78df6715817270 sio:SIO_000628 miriam-gene:25759 , lld:C0013264 ;
    a sio:SIO_001121 .
}
dgn-np:NP350428.RA1iizsrBGXyWLW_rQID7OhmvnvET_oopXBP5WYsSwpn4130_provenance {
  dgn-np:NP350428.RA1iizsrBGXyWLW_rQID7OhmvnvET_oopXBP5WYsSwpn4130_assertion dcterms:description "[Needle muscle biopsies from 14 genetically proven carriers of Duchenne muscular dystrophy (DMD), 14 possible carriers with elevated serum creatine kinase activity (SCK) and 37 possible carriers with normal SCK were compared with similar samples from 10 healthy volunteer females with the aim of identifying subtle changes that might aid carrier detection.]. 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:6452514 ;
    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:NP350428.RA1iizsrBGXyWLW_rQID7OhmvnvET_oopXBP5WYsSwpn4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:25+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" .
}