@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP62716.RA54Xk5vyPH-Ci-Uyholxd4Kp2F0VPvh-Dal-AlBffZnE> .
@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:NP62716.RA54Xk5vyPH-Ci-Uyholxd4Kp2F0VPvh-Dal-AlBffZnE130_head {
  this: np:hasAssertion dgn-np:NP62716.RA54Xk5vyPH-Ci-Uyholxd4Kp2F0VPvh-Dal-AlBffZnE130_assertion;
    np:hasProvenance dgn-np:NP62716.RA54Xk5vyPH-Ci-Uyholxd4Kp2F0VPvh-Dal-AlBffZnE130_provenance;
    np:hasPublicationInfo dgn-np:NP62716.RA54Xk5vyPH-Ci-Uyholxd4Kp2F0VPvh-Dal-AlBffZnE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP62716.RA54Xk5vyPH-Ci-Uyholxd4Kp2F0VPvh-Dal-AlBffZnE130_assertion a np:Assertion .
  
  dgn-np:NP62716.RA54Xk5vyPH-Ci-Uyholxd4Kp2F0VPvh-Dal-AlBffZnE130_provenance a np:Provenance .
  
  dgn-np:NP62716.RA54Xk5vyPH-Ci-Uyholxd4Kp2F0VPvh-Dal-AlBffZnE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP62716.RA54Xk5vyPH-Ci-Uyholxd4Kp2F0VPvh-Dal-AlBffZnE130_assertion {
  miriam-gene:22947 a ncit:C16612 .
  
  lld:C0026850 a ncit:C7057 .
  
  dgn-gda:DGN7ecaea3fb95fda5d885243b472cc7357 sio:SIO_000628 miriam-gene:22947, lld:C0026850;
    a sio:SIO_001122 .
}

dgn-np:NP62716.RA54Xk5vyPH-Ci-Uyholxd4Kp2F0VPvh-Dal-AlBffZnE130_provenance {
  dgn-np:NP62716.RA54Xk5vyPH-Ci-Uyholxd4Kp2F0VPvh-Dal-AlBffZnE130_assertion dcterms:description
      "[ The frequency of individuals having fewer numbers of D4Z4 repeats on chromosome 4q35 in Shanghai population is higher than that in Caucasian population although the short D4Z4 fragment on chromosome 4q35 is associated with facioscapulohumeral muscular dystrophy. These findings suggest that other factors may also contribute to facioscapulohumeral muscular dystrophy.]. 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:16086272;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP62716.RA54Xk5vyPH-Ci-Uyholxd4Kp2F0VPvh-Dal-AlBffZnE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:29+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" .
}