@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1180116.RAEHU54Vdcv79E8MkgqT3Iv3ZxFvXDF3EDgB6-0Z7H6mw> .
@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:NP1180116.RAEHU54Vdcv79E8MkgqT3Iv3ZxFvXDF3EDgB6-0Z7H6mw130_head {
  this: np:hasAssertion dgn-np:NP1180116.RAEHU54Vdcv79E8MkgqT3Iv3ZxFvXDF3EDgB6-0Z7H6mw130_assertion;
    np:hasProvenance dgn-np:NP1180116.RAEHU54Vdcv79E8MkgqT3Iv3ZxFvXDF3EDgB6-0Z7H6mw130_provenance;
    np:hasPublicationInfo dgn-np:NP1180116.RAEHU54Vdcv79E8MkgqT3Iv3ZxFvXDF3EDgB6-0Z7H6mw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1180116.RAEHU54Vdcv79E8MkgqT3Iv3ZxFvXDF3EDgB6-0Z7H6mw130_assertion a np:Assertion .
  
  dgn-np:NP1180116.RAEHU54Vdcv79E8MkgqT3Iv3ZxFvXDF3EDgB6-0Z7H6mw130_provenance a np:Provenance .
  
  dgn-np:NP1180116.RAEHU54Vdcv79E8MkgqT3Iv3ZxFvXDF3EDgB6-0Z7H6mw130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1180116.RAEHU54Vdcv79E8MkgqT3Iv3ZxFvXDF3EDgB6-0Z7H6mw130_assertion {
  miriam-gene:825 a ncit:C16612 .
  
  lld:C0026848 a ncit:C7057 .
  
  dgn-gda:DGNa67bf2e955254c3c3ec6fdd88e327440 sio:SIO_000628 miriam-gene:825, lld:C0026848;
    a sio:SIO_001121 .
}

dgn-np:NP1180116.RAEHU54Vdcv79E8MkgqT3Iv3ZxFvXDF3EDgB6-0Z7H6mw130_provenance {
  dgn-np:NP1180116.RAEHU54Vdcv79E8MkgqT3Iv3ZxFvXDF3EDgB6-0Z7H6mw130_assertion dcterms:description
      "[Number and location of eosinophils in skeletal muscle biopsies (n=100) was analysed by Giemsa and modified hematoxylin/eosin staining in patients with genetically confirmed myopathies (LGMD2A, LGMD2B, LGMD2L, facioscapulohumeral muscular dystrophy, dystrophinopathy), histologically confirmed idiopathic inflammatory myopathies (sporadic inclusion body myositis (sIBM), dermatomyositis (DM), polymyositis), amyotrophic lateral sclerosis (neurogenic control), and normal controls.]. 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:24803842;
    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:NP1180116.RAEHU54Vdcv79E8MkgqT3Iv3ZxFvXDF3EDgB6-0Z7H6mw130_publicationInfo {
  this: dcterms:created "2016-05-13T12:50:40+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:disgenetv3.0rdf;
    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" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}