@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP284815.RAAhcHf7Rpx_mF0HayEVRx1zIDU9Dqs8Jl74mDM5t6gco> .
@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:NP284815.RAAhcHf7Rpx_mF0HayEVRx1zIDU9Dqs8Jl74mDM5t6gco130_head {
  this: np:hasAssertion dgn-np:NP284815.RAAhcHf7Rpx_mF0HayEVRx1zIDU9Dqs8Jl74mDM5t6gco130_assertion;
    np:hasProvenance dgn-np:NP284815.RAAhcHf7Rpx_mF0HayEVRx1zIDU9Dqs8Jl74mDM5t6gco130_provenance;
    np:hasPublicationInfo dgn-np:NP284815.RAAhcHf7Rpx_mF0HayEVRx1zIDU9Dqs8Jl74mDM5t6gco130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP284815.RAAhcHf7Rpx_mF0HayEVRx1zIDU9Dqs8Jl74mDM5t6gco130_assertion a np:Assertion .
  
  dgn-np:NP284815.RAAhcHf7Rpx_mF0HayEVRx1zIDU9Dqs8Jl74mDM5t6gco130_provenance a np:Provenance .
  
  dgn-np:NP284815.RAAhcHf7Rpx_mF0HayEVRx1zIDU9Dqs8Jl74mDM5t6gco130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP284815.RAAhcHf7Rpx_mF0HayEVRx1zIDU9Dqs8Jl74mDM5t6gco130_assertion {
  miriam-gene:89 a ncit:C16612 .
  
  lld:C0017924 a ncit:C7057 .
  
  dgn-gda:DGN1a4dbbf3243019ee3c7d7c462355883c sio:SIO_000628 miriam-gene:89, lld:C0017924;
    a sio:SIO_001121 .
}

dgn-np:NP284815.RAAhcHf7Rpx_mF0HayEVRx1zIDU9Dqs8Jl74mDM5t6gco130_provenance {
  dgn-np:NP284815.RAAhcHf7Rpx_mF0HayEVRx1zIDU9Dqs8Jl74mDM5t6gco130_assertion dcterms:description
      "[We compared clinical presentation and exercise capacity between (i) four women with McArdle disease (aged 17, 36, 42 and 70 years) who were also carriers of the K153R variant in the myostatin (GDF-8) gene and in (ii) four women with this disorder matched forage (16, 33, 40 and 69 years), lifestyle, and documented genotype modulators of this disease (ACE, AMPD1 and ACTN3), who did not carry the myostatin variant.]. 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:19232494;
    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:NP284815.RAAhcHf7Rpx_mF0HayEVRx1zIDU9Dqs8Jl74mDM5t6gco130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:40+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" .
}