@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP972080.RAXFMEd331koTrXfZobKDBMi0A3d5wupCkfyteps1Hkbw> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP972080.RAXFMEd331koTrXfZobKDBMi0A3d5wupCkfyteps1Hkbw130_head {
  this: np:hasAssertion dgn-np:NP972080.RAXFMEd331koTrXfZobKDBMi0A3d5wupCkfyteps1Hkbw130_assertion;
    np:hasProvenance dgn-np:NP972080.RAXFMEd331koTrXfZobKDBMi0A3d5wupCkfyteps1Hkbw130_provenance;
    np:hasPublicationInfo dgn-np:NP972080.RAXFMEd331koTrXfZobKDBMi0A3d5wupCkfyteps1Hkbw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP972080.RAXFMEd331koTrXfZobKDBMi0A3d5wupCkfyteps1Hkbw130_assertion a np:Assertion .
  
  dgn-np:NP972080.RAXFMEd331koTrXfZobKDBMi0A3d5wupCkfyteps1Hkbw130_provenance a np:Provenance .
  
  dgn-np:NP972080.RAXFMEd331koTrXfZobKDBMi0A3d5wupCkfyteps1Hkbw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP972080.RAXFMEd331koTrXfZobKDBMi0A3d5wupCkfyteps1Hkbw130_assertion {
  miriam-gene:135228 a ncit:C16612 .
  
  lld:C0410174 a ncit:C7057 .
  
  dgn-gda:DGNcbda04fe4603efd4c7c5a9a0f549b7cd sio:SIO_000628 miriam-gene:135228, lld:C0410174;
    a sio:SIO_001121 .
}

dgn-np:NP972080.RAXFMEd331koTrXfZobKDBMi0A3d5wupCkfyteps1Hkbw130_provenance {
  dgn-np:NP972080.RAXFMEd331koTrXfZobKDBMi0A3d5wupCkfyteps1Hkbw130_assertion dcterms:description
      "[We presume that the deficiency of p180 in FCMD is caused specifically by the primary deficiency of fukutin, the causative protein of FCMD, and plays an important role in muscle cell degeneration in this disease.]. 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:11738352;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP972080.RAXFMEd331koTrXfZobKDBMi0A3d5wupCkfyteps1Hkbw130_publicationInfo {
  this: dcterms:created "2015-08-25T14:47:34+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}