@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1383060.RA_R4BMXpzbV_rR3NcyUy4IrjNHqTytZRo_HqTv5axi0I> .
@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:NP1383060.RA_R4BMXpzbV_rR3NcyUy4IrjNHqTytZRo_HqTv5axi0I130_head {
  this: np:hasAssertion dgn-np:NP1383060.RA_R4BMXpzbV_rR3NcyUy4IrjNHqTytZRo_HqTv5axi0I130_assertion ;
    np:hasProvenance dgn-np:NP1383060.RA_R4BMXpzbV_rR3NcyUy4IrjNHqTytZRo_HqTv5axi0I130_provenance ;
    np:hasPublicationInfo dgn-np:NP1383060.RA_R4BMXpzbV_rR3NcyUy4IrjNHqTytZRo_HqTv5axi0I130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP1383060.RA_R4BMXpzbV_rR3NcyUy4IrjNHqTytZRo_HqTv5axi0I130_assertion a np:Assertion .
  dgn-np:NP1383060.RA_R4BMXpzbV_rR3NcyUy4IrjNHqTytZRo_HqTv5axi0I130_provenance a np:Provenance .
  dgn-np:NP1383060.RA_R4BMXpzbV_rR3NcyUy4IrjNHqTytZRo_HqTv5axi0I130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP1383060.RA_R4BMXpzbV_rR3NcyUy4IrjNHqTytZRo_HqTv5axi0I130_assertion {
  miriam-gene:1760 a ncit:C16612 .
  lld:C0027126 a ncit:C7057 .
  dgn-gda:DGN4af7afc6a7c5eada5aab8852e477e85a sio:SIO_000628 miriam-gene:1760 , lld:C0027126 ;
    a sio:SIO_001121 .
}
dgn-np:NP1383060.RA_R4BMXpzbV_rR3NcyUy4IrjNHqTytZRo_HqTv5axi0I130_provenance {
  dgn-np:NP1383060.RA_R4BMXpzbV_rR3NcyUy4IrjNHqTytZRo_HqTv5axi0I130_assertion dcterms:description "[To investigate whether unusual allele segregation might explain the dominant negative effect of the expanded allele for myotonic dystrophy on myotonin protein kinase mRNA metabolism, which is suggested to cause the disease, we determined the number of CTG repeats at the DM locus in the nonaffected alleles of 64 DM (dystrophia myotonia) patients.]. 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:9353981 ;
    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:NP1383060.RA_R4BMXpzbV_rR3NcyUy4IrjNHqTytZRo_HqTv5axi0I130_publicationInfo {
  this: dcterms:created "2016-05-13T12:52:13+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
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    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" .
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}