@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP674512.RAKFsLcOz8R1HfSwId-E7Eg97VTTt9kb15OT1KLllxN_U> .
@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:NP674512.RAKFsLcOz8R1HfSwId-E7Eg97VTTt9kb15OT1KLllxN_U130_head {
  this: np:hasAssertion dgn-np:NP674512.RAKFsLcOz8R1HfSwId-E7Eg97VTTt9kb15OT1KLllxN_U130_assertion;
    np:hasProvenance dgn-np:NP674512.RAKFsLcOz8R1HfSwId-E7Eg97VTTt9kb15OT1KLllxN_U130_provenance;
    np:hasPublicationInfo dgn-np:NP674512.RAKFsLcOz8R1HfSwId-E7Eg97VTTt9kb15OT1KLllxN_U130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP674512.RAKFsLcOz8R1HfSwId-E7Eg97VTTt9kb15OT1KLllxN_U130_assertion a np:Assertion .
  
  dgn-np:NP674512.RAKFsLcOz8R1HfSwId-E7Eg97VTTt9kb15OT1KLllxN_U130_provenance a np:Provenance .
  
  dgn-np:NP674512.RAKFsLcOz8R1HfSwId-E7Eg97VTTt9kb15OT1KLllxN_U130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP674512.RAKFsLcOz8R1HfSwId-E7Eg97VTTt9kb15OT1KLllxN_U130_assertion {
  miriam-gene:2158 a ncit:C16612 .
  
  lld:C0026705 a ncit:C7057 .
  
  dgn-gda:DGN9d5005ed4c2743b5dc59a22133a043af sio:SIO_000628 miriam-gene:2158, lld:C0026705;
    a sio:SIO_001121 .
}

dgn-np:NP674512.RAKFsLcOz8R1HfSwId-E7Eg97VTTt9kb15OT1KLllxN_U130_provenance {
  dgn-np:NP674512.RAKFsLcOz8R1HfSwId-E7Eg97VTTt9kb15OT1KLllxN_U130_assertion dcterms:description
      "[By contrast, no significant differences were found in the recombination between 52A and factor IX in the two groups of MBS families or in these families versus those with Hunter syndrome examined in our laboratory.]. 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:3674751;
    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:NP674512.RAKFsLcOz8R1HfSwId-E7Eg97VTTt9kb15OT1KLllxN_U130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:47+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" .
}