@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP808404.RAlmdXhvFVa9dV5yB9rfuiRu4LIQ4zHH0ynRDMLYPmX8I> .
@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:NP808404.RAlmdXhvFVa9dV5yB9rfuiRu4LIQ4zHH0ynRDMLYPmX8I130_head {
  this: np:hasAssertion dgn-np:NP808404.RAlmdXhvFVa9dV5yB9rfuiRu4LIQ4zHH0ynRDMLYPmX8I130_assertion;
    np:hasProvenance dgn-np:NP808404.RAlmdXhvFVa9dV5yB9rfuiRu4LIQ4zHH0ynRDMLYPmX8I130_provenance;
    np:hasPublicationInfo dgn-np:NP808404.RAlmdXhvFVa9dV5yB9rfuiRu4LIQ4zHH0ynRDMLYPmX8I130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP808404.RAlmdXhvFVa9dV5yB9rfuiRu4LIQ4zHH0ynRDMLYPmX8I130_assertion a np:Assertion .
  
  dgn-np:NP808404.RAlmdXhvFVa9dV5yB9rfuiRu4LIQ4zHH0ynRDMLYPmX8I130_provenance a np:Provenance .
  
  dgn-np:NP808404.RAlmdXhvFVa9dV5yB9rfuiRu4LIQ4zHH0ynRDMLYPmX8I130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP808404.RAlmdXhvFVa9dV5yB9rfuiRu4LIQ4zHH0ynRDMLYPmX8I130_assertion {
  miriam-gene:27295 a ncit:C16612 .
  
  lld:C0238288 a ncit:C7057 .
  
  dgn-gda:DGNc152bf5745f592804a1444b6a049076d sio:SIO_000628 miriam-gene:27295, lld:C0238288;
    a sio:SIO_001121 .
}

dgn-np:NP808404.RAlmdXhvFVa9dV5yB9rfuiRu4LIQ4zHH0ynRDMLYPmX8I130_provenance {
  dgn-np:NP808404.RAlmdXhvFVa9dV5yB9rfuiRu4LIQ4zHH0ynRDMLYPmX8I130_assertion dcterms:description
      "[A total of 16 genes in the FSHD region (FRG2, TUBB4Q, FRG1, FAT1, F11, KLKB1, CYP4V2, TLR3, SORBS2, PDLIM3 (ALP), LRP2BP, ING2, SNX25, SLC25A4 (ANT1), HELT and IRF2) were examined for interallelic variation in RNA expression within individual myonuclei.]. 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:19888305;
    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 .
}

dgn-np:NP808404.RAlmdXhvFVa9dV5yB9rfuiRu4LIQ4zHH0ynRDMLYPmX8I130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:15+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" .
}