@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP692518.RAsUyALPY4_l4mlAhvu-xn7e9dTKT3IpIWyXYRkYz-XaE> .
@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:NP692518.RAsUyALPY4_l4mlAhvu-xn7e9dTKT3IpIWyXYRkYz-XaE130_head {
  this: np:hasAssertion dgn-np:NP692518.RAsUyALPY4_l4mlAhvu-xn7e9dTKT3IpIWyXYRkYz-XaE130_assertion;
    np:hasProvenance dgn-np:NP692518.RAsUyALPY4_l4mlAhvu-xn7e9dTKT3IpIWyXYRkYz-XaE130_provenance;
    np:hasPublicationInfo dgn-np:NP692518.RAsUyALPY4_l4mlAhvu-xn7e9dTKT3IpIWyXYRkYz-XaE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP692518.RAsUyALPY4_l4mlAhvu-xn7e9dTKT3IpIWyXYRkYz-XaE130_assertion a np:Assertion .
  
  dgn-np:NP692518.RAsUyALPY4_l4mlAhvu-xn7e9dTKT3IpIWyXYRkYz-XaE130_provenance a np:Provenance .
  
  dgn-np:NP692518.RAsUyALPY4_l4mlAhvu-xn7e9dTKT3IpIWyXYRkYz-XaE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP692518.RAsUyALPY4_l4mlAhvu-xn7e9dTKT3IpIWyXYRkYz-XaE130_assertion {
  miriam-gene:6445 a ncit:C16612 .
  
  lld:C2936331 a ncit:C7057 .
  
  dgn-gda:DGNb844f93ee1075f6aa48449fa9c275cfd sio:SIO_000628 miriam-gene:6445, lld:C2936331;
    a sio:SIO_001122 .
}

dgn-np:NP692518.RAsUyALPY4_l4mlAhvu-xn7e9dTKT3IpIWyXYRkYz-XaE130_provenance {
  dgn-np:NP692518.RAsUyALPY4_l4mlAhvu-xn7e9dTKT3IpIWyXYRkYz-XaE130_assertion dcterms:description
      "[This study, the first mutational analysis of Indian patients with sarcoglycanopathies suggests gamma SG mutations were the most common and the most prevalent mutation in the gamma SG gene was 525del T.]. 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:19770540;
    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:NP692518.RAsUyALPY4_l4mlAhvu-xn7e9dTKT3IpIWyXYRkYz-XaE130_publicationInfo {
  this: dcterms:created "2015-08-25T14:44:37+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" .
}