@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP754763.RAgkuj7abkT6zuWOCbKGz6HmXtdJ48PHB6e5XUWG-Q2kI> .
@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:NP754763.RAgkuj7abkT6zuWOCbKGz6HmXtdJ48PHB6e5XUWG-Q2kI130_head {
  this: np:hasAssertion dgn-np:NP754763.RAgkuj7abkT6zuWOCbKGz6HmXtdJ48PHB6e5XUWG-Q2kI130_assertion ;
    np:hasProvenance dgn-np:NP754763.RAgkuj7abkT6zuWOCbKGz6HmXtdJ48PHB6e5XUWG-Q2kI130_provenance ;
    np:hasPublicationInfo dgn-np:NP754763.RAgkuj7abkT6zuWOCbKGz6HmXtdJ48PHB6e5XUWG-Q2kI130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP754763.RAgkuj7abkT6zuWOCbKGz6HmXtdJ48PHB6e5XUWG-Q2kI130_assertion a np:Assertion .
  dgn-np:NP754763.RAgkuj7abkT6zuWOCbKGz6HmXtdJ48PHB6e5XUWG-Q2kI130_provenance a np:Provenance .
  dgn-np:NP754763.RAgkuj7abkT6zuWOCbKGz6HmXtdJ48PHB6e5XUWG-Q2kI130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP754763.RAgkuj7abkT6zuWOCbKGz6HmXtdJ48PHB6e5XUWG-Q2kI130_assertion {
  miriam-gene:4659 a ncit:C16612 .
  lld:C0025362 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP754763.RAgkuj7abkT6zuWOCbKGz6HmXtdJ48PHB6e5XUWG-Q2kI130_provenance {
  dgn-np:NP754763.RAgkuj7abkT6zuWOCbKGz6HmXtdJ48PHB6e5XUWG-Q2kI130_assertion dcterms:description "[In order to test whether the direct molecular diagnostic approach for fragile X mental retardation (Martin-Bell syndrome, MBS) really makes diagnosis of this disease more precise, we evaluated the results of direct diagnosis in 40 German families at risk together with the results of an earlier study with closely linked flanking markers in the same families.]. 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:8097256 ;
    prov:wasDerivedFrom dgn-void:befree-20140225 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^xsd:date .
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    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ;
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dgn-np:NP754763.RAgkuj7abkT6zuWOCbKGz6HmXtdJ48PHB6e5XUWG-Q2kI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:37+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
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