@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP797533.RANdWf5bXXHXiN2rt5ciqsETgTmoFPjMNsDCpxyNQ-Wos> .
@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:NP797533.RANdWf5bXXHXiN2rt5ciqsETgTmoFPjMNsDCpxyNQ-Wos130_head {
  this: np:hasAssertion dgn-np:NP797533.RANdWf5bXXHXiN2rt5ciqsETgTmoFPjMNsDCpxyNQ-Wos130_assertion;
    np:hasProvenance dgn-np:NP797533.RANdWf5bXXHXiN2rt5ciqsETgTmoFPjMNsDCpxyNQ-Wos130_provenance;
    np:hasPublicationInfo dgn-np:NP797533.RANdWf5bXXHXiN2rt5ciqsETgTmoFPjMNsDCpxyNQ-Wos130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP797533.RANdWf5bXXHXiN2rt5ciqsETgTmoFPjMNsDCpxyNQ-Wos130_assertion a np:Assertion .
  
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  dgn-np:NP797533.RANdWf5bXXHXiN2rt5ciqsETgTmoFPjMNsDCpxyNQ-Wos130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP797533.RANdWf5bXXHXiN2rt5ciqsETgTmoFPjMNsDCpxyNQ-Wos130_assertion {
  miriam-gene:2273 a ncit:C16612 .
  
  lld:C1834673 a ncit:C7057 .
  
  dgn-gda:DGNd56f8df0b9a039929e685914fafd1cc5 sio:SIO_000628 miriam-gene:2273, lld:C1834673;
    a sio:SIO_001121 .
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dgn-np:NP797533.RANdWf5bXXHXiN2rt5ciqsETgTmoFPjMNsDCpxyNQ-Wos130_provenance {
  dgn-np:NP797533.RANdWf5bXXHXiN2rt5ciqsETgTmoFPjMNsDCpxyNQ-Wos130_assertion dcterms:description
      "[The authors identified one patient carrying a complex rearrangement in the FSHD locus that masked the D4Z4 contraction associated with FSHD1 in standard genetic testing, one patient with somatic mosaicism for the D4Z4 4q35 contraction, six patients that were diagnosed as having FSHD2, four patients with CAPN3 mutations and two patients with a VCP mutation, No mutations were detected in FHL1, and in two patients, the authors could not identify the genetic defect.]. 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:21984748;
    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:NP797533.RANdWf5bXXHXiN2rt5ciqsETgTmoFPjMNsDCpxyNQ-Wos130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:09+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" .
}