@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP283113.RA49ClQzr84bTlh-Uhd3FN9iCRIaZGc4ED3rO02874orA> .
@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#> .
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  this: np:hasAssertion dgn-np:NP283113.RA49ClQzr84bTlh-Uhd3FN9iCRIaZGc4ED3rO02874orA130_assertion ;
    np:hasProvenance dgn-np:NP283113.RA49ClQzr84bTlh-Uhd3FN9iCRIaZGc4ED3rO02874orA130_provenance ;
    np:hasPublicationInfo dgn-np:NP283113.RA49ClQzr84bTlh-Uhd3FN9iCRIaZGc4ED3rO02874orA130_publicationInfo ;
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  dgn-np:NP283113.RA49ClQzr84bTlh-Uhd3FN9iCRIaZGc4ED3rO02874orA130_provenance a np:Provenance .
  dgn-np:NP283113.RA49ClQzr84bTlh-Uhd3FN9iCRIaZGc4ED3rO02874orA130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP283113.RA49ClQzr84bTlh-Uhd3FN9iCRIaZGc4ED3rO02874orA130_assertion {
  miriam-gene:1760 a ncit:C16612 .
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dgn-np:NP283113.RA49ClQzr84bTlh-Uhd3FN9iCRIaZGc4ED3rO02874orA130_provenance {
  dgn-np:NP283113.RA49ClQzr84bTlh-Uhd3FN9iCRIaZGc4ED3rO02874orA130_assertion dcterms:description "[We compared the magnetic resonance imaging derived grey matter maps of 22 DM1 patients with those of matched, healthy controls using voxel based morphometry to evaluate the extension of global and regional cortical atrophy in DM1, as well as its relationships with clinical and genetic features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
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    prov:wasDerivedFrom dgn-void:befree-20140225 ;
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  dgn-void:source_evidence_literature a eco:ECO_0000212 ;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ;
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dgn-np:NP283113.RA49ClQzr84bTlh-Uhd3FN9iCRIaZGc4ED3rO02874orA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:39+02:00"^^xsd:dateTime ;
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