@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP786007.RA9O5l8AMxTVLpxcvY7v2NgLJE0ujjR-Q8U6lW4Z_6rV8> .
@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:NP786007.RA9O5l8AMxTVLpxcvY7v2NgLJE0ujjR-Q8U6lW4Z_6rV8130_head {
  this: np:hasAssertion dgn-np:NP786007.RA9O5l8AMxTVLpxcvY7v2NgLJE0ujjR-Q8U6lW4Z_6rV8130_assertion;
    np:hasProvenance dgn-np:NP786007.RA9O5l8AMxTVLpxcvY7v2NgLJE0ujjR-Q8U6lW4Z_6rV8130_provenance;
    np:hasPublicationInfo dgn-np:NP786007.RA9O5l8AMxTVLpxcvY7v2NgLJE0ujjR-Q8U6lW4Z_6rV8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP786007.RA9O5l8AMxTVLpxcvY7v2NgLJE0ujjR-Q8U6lW4Z_6rV8130_assertion a np:Assertion .
  
  dgn-np:NP786007.RA9O5l8AMxTVLpxcvY7v2NgLJE0ujjR-Q8U6lW4Z_6rV8130_provenance a np:Provenance .
  
  dgn-np:NP786007.RA9O5l8AMxTVLpxcvY7v2NgLJE0ujjR-Q8U6lW4Z_6rV8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP786007.RA9O5l8AMxTVLpxcvY7v2NgLJE0ujjR-Q8U6lW4Z_6rV8130_assertion {
  miriam-gene:6288 a ncit:C16612 .
  
  lld:C1838022 a ncit:C7057 .
  
  dgn-gda:DGN2dcac168532e1ff2cf708d014de286be sio:SIO_000628 miriam-gene:6288, lld:C1838022;
    a sio:SIO_001121 .
}

dgn-np:NP786007.RA9O5l8AMxTVLpxcvY7v2NgLJE0ujjR-Q8U6lW4Z_6rV8130_provenance {
  dgn-np:NP786007.RA9O5l8AMxTVLpxcvY7v2NgLJE0ujjR-Q8U6lW4Z_6rV8130_assertion dcterms:description
      "[A significant difference in the frequency of the A1 allele was found among these three groups of boys, with the SAA group having the highest A1 allele frequency (.313), followed by the SRA (.139) and the SSD (.133) groups.]. 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:8128963;
    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:NP786007.RA9O5l8AMxTVLpxcvY7v2NgLJE0ujjR-Q8U6lW4Z_6rV8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:56+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" .
}