@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP43902.RA83ctCIxQVtIMjYqzf3ttpAI1UFqbftTL2wSSGJ2Nwm0> .
@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:NP43902.RA83ctCIxQVtIMjYqzf3ttpAI1UFqbftTL2wSSGJ2Nwm0130_head {
  this: np:hasAssertion dgn-np:NP43902.RA83ctCIxQVtIMjYqzf3ttpAI1UFqbftTL2wSSGJ2Nwm0130_assertion;
    np:hasProvenance dgn-np:NP43902.RA83ctCIxQVtIMjYqzf3ttpAI1UFqbftTL2wSSGJ2Nwm0130_provenance;
    np:hasPublicationInfo dgn-np:NP43902.RA83ctCIxQVtIMjYqzf3ttpAI1UFqbftTL2wSSGJ2Nwm0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP43902.RA83ctCIxQVtIMjYqzf3ttpAI1UFqbftTL2wSSGJ2Nwm0130_assertion a np:Assertion .
  
  dgn-np:NP43902.RA83ctCIxQVtIMjYqzf3ttpAI1UFqbftTL2wSSGJ2Nwm0130_provenance a np:Provenance .
  
  dgn-np:NP43902.RA83ctCIxQVtIMjYqzf3ttpAI1UFqbftTL2wSSGJ2Nwm0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP43902.RA83ctCIxQVtIMjYqzf3ttpAI1UFqbftTL2wSSGJ2Nwm0130_assertion {
  miriam-gene:2332 a ncit:C16612 .
  
  lld:C0085215 a ncit:C7057 .
  
  dgn-gda:DGNcdb3d5289112b6e43ae309ed7cf007a5 sio:SIO_000628 miriam-gene:2332, lld:C0085215;
    a sio:SIO_001122 .
}

dgn-np:NP43902.RA83ctCIxQVtIMjYqzf3ttpAI1UFqbftTL2wSSGJ2Nwm0130_provenance {
  dgn-np:NP43902.RA83ctCIxQVtIMjYqzf3ttpAI1UFqbftTL2wSSGJ2Nwm0130_assertion dcterms:description
      "[The results of our research confirm the actuality of genetic tests of mutations in INHalpha1 and FMR1 genes among the women of reproductive age with the purpose of POF prognosis and prevention the birth of children with fragile X syndrome.]. 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:16161415;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP43902.RA83ctCIxQVtIMjYqzf3ttpAI1UFqbftTL2wSSGJ2Nwm0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:20+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" .
}