@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP858882.RAtCPfwyyhlaxO38fUoAOMtcoa2fE4Pldw2ghedj8w3tc> .
@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:NP858882.RAtCPfwyyhlaxO38fUoAOMtcoa2fE4Pldw2ghedj8w3tc130_head {
  this: np:hasAssertion dgn-np:NP858882.RAtCPfwyyhlaxO38fUoAOMtcoa2fE4Pldw2ghedj8w3tc130_assertion;
    np:hasProvenance dgn-np:NP858882.RAtCPfwyyhlaxO38fUoAOMtcoa2fE4Pldw2ghedj8w3tc130_provenance;
    np:hasPublicationInfo dgn-np:NP858882.RAtCPfwyyhlaxO38fUoAOMtcoa2fE4Pldw2ghedj8w3tc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP858882.RAtCPfwyyhlaxO38fUoAOMtcoa2fE4Pldw2ghedj8w3tc130_assertion a np:Assertion .
  
  dgn-np:NP858882.RAtCPfwyyhlaxO38fUoAOMtcoa2fE4Pldw2ghedj8w3tc130_provenance a np:Provenance .
  
  dgn-np:NP858882.RAtCPfwyyhlaxO38fUoAOMtcoa2fE4Pldw2ghedj8w3tc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP858882.RAtCPfwyyhlaxO38fUoAOMtcoa2fE4Pldw2ghedj8w3tc130_assertion {
  miriam-gene:9429 a ncit:C16612 .
  
  lld:C0025362 a ncit:C7057 .
  
  dgn-gda:DGN74cff7a02dd29a322065877f42453f0e sio:SIO_000628 miriam-gene:9429, lld:C0025362;
    a sio:SIO_001121 .
}

dgn-np:NP858882.RAtCPfwyyhlaxO38fUoAOMtcoa2fE4Pldw2ghedj8w3tc130_provenance {
  dgn-np:NP858882.RAtCPfwyyhlaxO38fUoAOMtcoa2fE4Pldw2ghedj8w3tc130_assertion dcterms:description
      "[Given that there are other eight MRX families overlapping this interval, none of them with known mutation, we conclude that at least one new gene responsible for nonsyndromic mental retardation is located in this region.]. 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:15526294;
    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:NP858882.RAtCPfwyyhlaxO38fUoAOMtcoa2fE4Pldw2ghedj8w3tc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:45+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" .
}