@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP636137.RAPbFK_lwqJDqa_OjERqFcDUfcfoSzelvvKTPadV7QVyw> .
@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:NP636137.RAPbFK_lwqJDqa_OjERqFcDUfcfoSzelvvKTPadV7QVyw130_head {
  this: np:hasAssertion dgn-np:NP636137.RAPbFK_lwqJDqa_OjERqFcDUfcfoSzelvvKTPadV7QVyw130_assertion;
    np:hasProvenance dgn-np:NP636137.RAPbFK_lwqJDqa_OjERqFcDUfcfoSzelvvKTPadV7QVyw130_provenance;
    np:hasPublicationInfo dgn-np:NP636137.RAPbFK_lwqJDqa_OjERqFcDUfcfoSzelvvKTPadV7QVyw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP636137.RAPbFK_lwqJDqa_OjERqFcDUfcfoSzelvvKTPadV7QVyw130_assertion a np:Assertion .
  
  dgn-np:NP636137.RAPbFK_lwqJDqa_OjERqFcDUfcfoSzelvvKTPadV7QVyw130_provenance a np:Provenance .
  
  dgn-np:NP636137.RAPbFK_lwqJDqa_OjERqFcDUfcfoSzelvvKTPadV7QVyw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP636137.RAPbFK_lwqJDqa_OjERqFcDUfcfoSzelvvKTPadV7QVyw130_assertion {
  miriam-gene:26227 a ncit:C16612 .
  
  lld:C0008626 a ncit:C7057 .
  
  dgn-gda:DGNe20658848ba8ac5284d9654e5cd298ed sio:SIO_000628 miriam-gene:26227, lld:C0008626;
    a sio:SIO_001121 .
}

dgn-np:NP636137.RAPbFK_lwqJDqa_OjERqFcDUfcfoSzelvvKTPadV7QVyw130_provenance {
  dgn-np:NP636137.RAPbFK_lwqJDqa_OjERqFcDUfcfoSzelvvKTPadV7QVyw130_assertion dcterms:description
      "[In order to establish a simple and useful way for preimplantation genetic diagnosis (PGD) of chromosomal diseases in general IVF laboratory, the methods that are most commonly used in the embryo biopsy, fixation of blastomere and fluorescence in situ hybridization were compared.]. 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:17641851;
    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:NP636137.RAPbFK_lwqJDqa_OjERqFcDUfcfoSzelvvKTPadV7QVyw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:23+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" .
}