@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP652044.RAQf8dv5EvFkv_bUCYrD4kEhx5pWUPvoWZAOm3z1yQTok> .
@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:NP652044.RAQf8dv5EvFkv_bUCYrD4kEhx5pWUPvoWZAOm3z1yQTok130_head {
  this: np:hasAssertion dgn-np:NP652044.RAQf8dv5EvFkv_bUCYrD4kEhx5pWUPvoWZAOm3z1yQTok130_assertion;
    np:hasProvenance dgn-np:NP652044.RAQf8dv5EvFkv_bUCYrD4kEhx5pWUPvoWZAOm3z1yQTok130_provenance;
    np:hasPublicationInfo dgn-np:NP652044.RAQf8dv5EvFkv_bUCYrD4kEhx5pWUPvoWZAOm3z1yQTok130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP652044.RAQf8dv5EvFkv_bUCYrD4kEhx5pWUPvoWZAOm3z1yQTok130_assertion a np:Assertion .
  
  dgn-np:NP652044.RAQf8dv5EvFkv_bUCYrD4kEhx5pWUPvoWZAOm3z1yQTok130_provenance a np:Provenance .
  
  dgn-np:NP652044.RAQf8dv5EvFkv_bUCYrD4kEhx5pWUPvoWZAOm3z1yQTok130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP652044.RAQf8dv5EvFkv_bUCYrD4kEhx5pWUPvoWZAOm3z1yQTok130_assertion {
  miriam-gene:6520 a ncit:C16612 .
  
  lld:C0026848 a ncit:C7057 .
  
  dgn-gda:DGNa60f46fffbae6b156bacfe8a0b6caddc sio:SIO_000628 miriam-gene:6520, lld:C0026848;
    a sio:SIO_001121 .
}

dgn-np:NP652044.RAQf8dv5EvFkv_bUCYrD4kEhx5pWUPvoWZAOm3z1yQTok130_provenance {
  dgn-np:NP652044.RAQf8dv5EvFkv_bUCYrD4kEhx5pWUPvoWZAOm3z1yQTok130_assertion dcterms:description
      "[The lack of different proteins accruing, but the mutant ones at an early age of affected patients in actin filament aggregating myopathy (AFAM) and hyaline body myopathy (HBM), suggests defects in maturation of sarcomeres and failure to integrate the possible mutant proteins, sarcomeric actin and heavy chain myosin in AFAM and HBM, a disturbance of anabolic metabolism.]. 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:22172423;
    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:NP652044.RAQf8dv5EvFkv_bUCYrD4kEhx5pWUPvoWZAOm3z1yQTok130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:33+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" .
}