@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP833993.RASU6MRprNHH8EPm8fff75c_swbbgOZvYECLbSGL19n7M> .
@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:NP833993.RASU6MRprNHH8EPm8fff75c_swbbgOZvYECLbSGL19n7M130_head {
  this: np:hasAssertion dgn-np:NP833993.RASU6MRprNHH8EPm8fff75c_swbbgOZvYECLbSGL19n7M130_assertion;
    np:hasProvenance dgn-np:NP833993.RASU6MRprNHH8EPm8fff75c_swbbgOZvYECLbSGL19n7M130_provenance;
    np:hasPublicationInfo dgn-np:NP833993.RASU6MRprNHH8EPm8fff75c_swbbgOZvYECLbSGL19n7M130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP833993.RASU6MRprNHH8EPm8fff75c_swbbgOZvYECLbSGL19n7M130_assertion a np:Assertion .
  
  dgn-np:NP833993.RASU6MRprNHH8EPm8fff75c_swbbgOZvYECLbSGL19n7M130_provenance a np:Provenance .
  
  dgn-np:NP833993.RASU6MRprNHH8EPm8fff75c_swbbgOZvYECLbSGL19n7M130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP833993.RASU6MRprNHH8EPm8fff75c_swbbgOZvYECLbSGL19n7M130_assertion {
  miriam-gene:2489 a ncit:C16612 .
  
  lld:C0581883 a ncit:C7057 .
  
  dgn-gda:DGN2aac6c15d1c56a86b8ea94616d12d714 sio:SIO_000628 miriam-gene:2489, lld:C0581883;
    a sio:SIO_001121 .
}

dgn-np:NP833993.RASU6MRprNHH8EPm8fff75c_swbbgOZvYECLbSGL19n7M130_provenance {
  dgn-np:NP833993.RASU6MRprNHH8EPm8fff75c_swbbgOZvYECLbSGL19n7M130_assertion dcterms:description
      "[FAT1 lies near the critical locus involved in causing FSHD, and Fat1 mutant mice also show retinal vasculopathy, mimicking another symptom of FSHD, and showed abnormal inner ear patterning, predictive of deafness, reminiscent of another burden of FSHD.]. 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:23785297;
    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:NP833993.RASU6MRprNHH8EPm8fff75c_swbbgOZvYECLbSGL19n7M130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:30+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" .
}