@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP429570.RASvE-IPgrM7iwUHlHKxAk62i4wiEP9JuT3UWIcbgaE7M> .
@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:NP429570.RASvE-IPgrM7iwUHlHKxAk62i4wiEP9JuT3UWIcbgaE7M130_head {
  this: np:hasAssertion dgn-np:NP429570.RASvE-IPgrM7iwUHlHKxAk62i4wiEP9JuT3UWIcbgaE7M130_assertion;
    np:hasProvenance dgn-np:NP429570.RASvE-IPgrM7iwUHlHKxAk62i4wiEP9JuT3UWIcbgaE7M130_provenance;
    np:hasPublicationInfo dgn-np:NP429570.RASvE-IPgrM7iwUHlHKxAk62i4wiEP9JuT3UWIcbgaE7M130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP429570.RASvE-IPgrM7iwUHlHKxAk62i4wiEP9JuT3UWIcbgaE7M130_assertion a np:Assertion .
  
  dgn-np:NP429570.RASvE-IPgrM7iwUHlHKxAk62i4wiEP9JuT3UWIcbgaE7M130_provenance a np:Provenance .
  
  dgn-np:NP429570.RASvE-IPgrM7iwUHlHKxAk62i4wiEP9JuT3UWIcbgaE7M130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP429570.RASvE-IPgrM7iwUHlHKxAk62i4wiEP9JuT3UWIcbgaE7M130_assertion {
  miriam-gene:6442 a ncit:C16612 .
  
  lld:C0410173 a ncit:C7057 .
  
  dgn-gda:DGN2dac36fe2d21ca539f534dbe12d38f15 sio:SIO_000628 miriam-gene:6442, lld:C0410173;
    a sio:SIO_001121 .
}

dgn-np:NP429570.RASvE-IPgrM7iwUHlHKxAk62i4wiEP9JuT3UWIcbgaE7M130_provenance {
  dgn-np:NP429570.RASvE-IPgrM7iwUHlHKxAk62i4wiEP9JuT3UWIcbgaE7M130_assertion dcterms:description
      "[It has been previously shown in Tunisian and Algerian families that the locus for SCARMD maps to the proximal part of 13q, and in Algerian families that the disease is associated with deficiency of the 50 kDa dystrophin associated glycoprotein (50DAG).]. 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:8071965;
    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:NP429570.RASvE-IPgrM7iwUHlHKxAk62i4wiEP9JuT3UWIcbgaE7M130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:14+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" .
}