@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP358702.RAGpEZWvsNnF_YI7ozr5bcVqFCLCPuhfVNkaQIceXmVIQ> .
@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:NP358702.RAGpEZWvsNnF_YI7ozr5bcVqFCLCPuhfVNkaQIceXmVIQ130_head {
  this: np:hasAssertion dgn-np:NP358702.RAGpEZWvsNnF_YI7ozr5bcVqFCLCPuhfVNkaQIceXmVIQ130_assertion;
    np:hasProvenance dgn-np:NP358702.RAGpEZWvsNnF_YI7ozr5bcVqFCLCPuhfVNkaQIceXmVIQ130_provenance;
    np:hasPublicationInfo dgn-np:NP358702.RAGpEZWvsNnF_YI7ozr5bcVqFCLCPuhfVNkaQIceXmVIQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP358702.RAGpEZWvsNnF_YI7ozr5bcVqFCLCPuhfVNkaQIceXmVIQ130_assertion a np:Assertion .
  
  dgn-np:NP358702.RAGpEZWvsNnF_YI7ozr5bcVqFCLCPuhfVNkaQIceXmVIQ130_provenance a np:Provenance .
  
  dgn-np:NP358702.RAGpEZWvsNnF_YI7ozr5bcVqFCLCPuhfVNkaQIceXmVIQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP358702.RAGpEZWvsNnF_YI7ozr5bcVqFCLCPuhfVNkaQIceXmVIQ130_assertion {
  miriam-gene:9499 a ncit:C16612 .
  
  lld:C0026848 a ncit:C7057 .
  
  dgn-gda:DGNf953fbed1cdd1e433bfc137d70d206df sio:SIO_000628 miriam-gene:9499, lld:C0026848;
    a sio:SIO_001121 .
}

dgn-np:NP358702.RAGpEZWvsNnF_YI7ozr5bcVqFCLCPuhfVNkaQIceXmVIQ130_provenance {
  dgn-np:NP358702.RAGpEZWvsNnF_YI7ozr5bcVqFCLCPuhfVNkaQIceXmVIQ130_assertion dcterms:description
      "[The essential role of myotilin in skeletal muscle is attested by the observation that certain forms of myofibrillar myopathy and limb girdle muscular dystrophy are caused by mutations in the human myotilin gene.]. 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:16076904;
    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:NP358702.RAGpEZWvsNnF_YI7ozr5bcVqFCLCPuhfVNkaQIceXmVIQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:30+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" .
}