@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP815109.RAMuqHgzNFEpbXkoClvQ4JfCSOK45hBRBVV7pYaHd_eHs> .
@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:NP815109.RAMuqHgzNFEpbXkoClvQ4JfCSOK45hBRBVV7pYaHd_eHs130_head {
  this: np:hasAssertion dgn-np:NP815109.RAMuqHgzNFEpbXkoClvQ4JfCSOK45hBRBVV7pYaHd_eHs130_assertion;
    np:hasProvenance dgn-np:NP815109.RAMuqHgzNFEpbXkoClvQ4JfCSOK45hBRBVV7pYaHd_eHs130_provenance;
    np:hasPublicationInfo dgn-np:NP815109.RAMuqHgzNFEpbXkoClvQ4JfCSOK45hBRBVV7pYaHd_eHs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP815109.RAMuqHgzNFEpbXkoClvQ4JfCSOK45hBRBVV7pYaHd_eHs130_assertion a np:Assertion .
  
  dgn-np:NP815109.RAMuqHgzNFEpbXkoClvQ4JfCSOK45hBRBVV7pYaHd_eHs130_provenance a np:Provenance .
  
  dgn-np:NP815109.RAMuqHgzNFEpbXkoClvQ4JfCSOK45hBRBVV7pYaHd_eHs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP815109.RAMuqHgzNFEpbXkoClvQ4JfCSOK45hBRBVV7pYaHd_eHs130_assertion {
  miriam-gene:353322 a ncit:C16612 .
  
  lld:C0238288 a ncit:C7057 .
  
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    a sio:SIO_001121 .
}

dgn-np:NP815109.RAMuqHgzNFEpbXkoClvQ4JfCSOK45hBRBVV7pYaHd_eHs130_provenance {
  dgn-np:NP815109.RAMuqHgzNFEpbXkoClvQ4JfCSOK45hBRBVV7pYaHd_eHs130_assertion dcterms:description
      "[The aim of this study is to comprehensively and uniformly study the expression of the FSHD candidate genes FRG1, FRG2, CRYM, ANT1, ALP, PITX1 and LRP2BP at the RNA and protein level in identically processed primary myoblasts, myotubes and quadriceps muscle.]. 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:19809486;
    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:NP815109.RAMuqHgzNFEpbXkoClvQ4JfCSOK45hBRBVV7pYaHd_eHs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:19+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>,
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}