@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP528682.RAyjh1hmWuS0YyWYxAtEzSrG6lvkwN1AKM6cEQEMufvLg> .
@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:NP528682.RAyjh1hmWuS0YyWYxAtEzSrG6lvkwN1AKM6cEQEMufvLg130_head {
   this: np:hasAssertion dgn-np:NP528682.RAyjh1hmWuS0YyWYxAtEzSrG6lvkwN1AKM6cEQEMufvLg130_assertion ;
    np:hasProvenance dgn-np:NP528682.RAyjh1hmWuS0YyWYxAtEzSrG6lvkwN1AKM6cEQEMufvLg130_provenance ;
    np:hasPublicationInfo dgn-np:NP528682.RAyjh1hmWuS0YyWYxAtEzSrG6lvkwN1AKM6cEQEMufvLg130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP528682.RAyjh1hmWuS0YyWYxAtEzSrG6lvkwN1AKM6cEQEMufvLg130_assertion a np:Assertion .
  dgn-np:NP528682.RAyjh1hmWuS0YyWYxAtEzSrG6lvkwN1AKM6cEQEMufvLg130_provenance a np:Provenance .
  dgn-np:NP528682.RAyjh1hmWuS0YyWYxAtEzSrG6lvkwN1AKM6cEQEMufvLg130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP528682.RAyjh1hmWuS0YyWYxAtEzSrG6lvkwN1AKM6cEQEMufvLg130_assertion {
   miriam-gene:825 a ncit:C16612 .
  lld:C2936331 a ncit:C7057 .
  dgn-gda:DGNb33a814f5128a6bf1d72fbce66a81da2 sio:SIO_000628 miriam-gene:825 , lld:C2936331 ;
    a sio:SIO_001121 .
}
dgn-np:NP528682.RAyjh1hmWuS0YyWYxAtEzSrG6lvkwN1AKM6cEQEMufvLg130_provenance {
   dgn-np:NP528682.RAyjh1hmWuS0YyWYxAtEzSrG6lvkwN1AKM6cEQEMufvLg130_assertion dcterms:description "[In this study, we investigated the proteolysis of beta-dystroglycan in the biopsied skeletal muscles of various human muscular diseases, including sarcoglycanopathy, Duchenne muscular dystrophy (DMD), Becker muscular dystrophy, Fukuyama congenital muscular dystrophy, Miyoshi myopathy, LGMD2A, facioscapulohumeral muscular dystrophy, myotonic dystrophy and dermatomyositis/polymyositis.]. 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:15833425 ;
    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 .
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dgn-np:NP528682.RAyjh1hmWuS0YyWYxAtEzSrG6lvkwN1AKM6cEQEMufvLg130_publicationInfo {
   this: dcterms:created "2014-10-02T12:37:19+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> ;
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}