@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP359128.RASx1F6Ovu1g5qgmu5WLNiYdVGxo_IYUT9RbaSdt_tDs4> .
@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:NP359128.RASx1F6Ovu1g5qgmu5WLNiYdVGxo_IYUT9RbaSdt_tDs4130_head {
  this: np:hasAssertion dgn-np:NP359128.RASx1F6Ovu1g5qgmu5WLNiYdVGxo_IYUT9RbaSdt_tDs4130_assertion;
    np:hasProvenance dgn-np:NP359128.RASx1F6Ovu1g5qgmu5WLNiYdVGxo_IYUT9RbaSdt_tDs4130_provenance;
    np:hasPublicationInfo dgn-np:NP359128.RASx1F6Ovu1g5qgmu5WLNiYdVGxo_IYUT9RbaSdt_tDs4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP359128.RASx1F6Ovu1g5qgmu5WLNiYdVGxo_IYUT9RbaSdt_tDs4130_assertion a np:Assertion .
  
  dgn-np:NP359128.RASx1F6Ovu1g5qgmu5WLNiYdVGxo_IYUT9RbaSdt_tDs4130_provenance a np:Provenance .
  
  dgn-np:NP359128.RASx1F6Ovu1g5qgmu5WLNiYdVGxo_IYUT9RbaSdt_tDs4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP359128.RASx1F6Ovu1g5qgmu5WLNiYdVGxo_IYUT9RbaSdt_tDs4130_assertion {
  miriam-gene:84162 a ncit:C16612 .
  
  lld:C1136249 a ncit:C7057 .
  
  dgn-gda:DGN9c625ebc511bf98accf2375d809b6969 sio:SIO_000628 miriam-gene:84162, lld:C1136249;
    a sio:SIO_001121 .
}

dgn-np:NP359128.RASx1F6Ovu1g5qgmu5WLNiYdVGxo_IYUT9RbaSdt_tDs4130_provenance {
  dgn-np:NP359128.RASx1F6Ovu1g5qgmu5WLNiYdVGxo_IYUT9RbaSdt_tDs4130_assertion dcterms:description
      "[These observations and the well-established knowledge that the genes for Deutan and Protan colorblindness are closely linked to G6PD, but segregate independently of factor IX deficiency, suggest that the fragile site associated with this type of X-linked mental retardation occurs in a region prone to high frequency of meiotic recombination.]. 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:6595664;
    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:NP359128.RASx1F6Ovu1g5qgmu5WLNiYdVGxo_IYUT9RbaSdt_tDs4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:30+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" .
}