@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP851639.RAeYMey7KUCmkUyULIlU3BV2aV-KPwfZHP5sxar7bw6iU> .
@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:NP851639.RAeYMey7KUCmkUyULIlU3BV2aV-KPwfZHP5sxar7bw6iU130_head {
  this: np:hasAssertion dgn-np:NP851639.RAeYMey7KUCmkUyULIlU3BV2aV-KPwfZHP5sxar7bw6iU130_assertion ;
    np:hasProvenance dgn-np:NP851639.RAeYMey7KUCmkUyULIlU3BV2aV-KPwfZHP5sxar7bw6iU130_provenance ;
    np:hasPublicationInfo dgn-np:NP851639.RAeYMey7KUCmkUyULIlU3BV2aV-KPwfZHP5sxar7bw6iU130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP851639.RAeYMey7KUCmkUyULIlU3BV2aV-KPwfZHP5sxar7bw6iU130_assertion a np:Assertion .
  dgn-np:NP851639.RAeYMey7KUCmkUyULIlU3BV2aV-KPwfZHP5sxar7bw6iU130_provenance a np:Provenance .
  dgn-np:NP851639.RAeYMey7KUCmkUyULIlU3BV2aV-KPwfZHP5sxar7bw6iU130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP851639.RAeYMey7KUCmkUyULIlU3BV2aV-KPwfZHP5sxar7bw6iU130_assertion {
  miriam-gene:4163 a ncit:C16612 .
  lld:C0007129 a ncit:C7057 .
  dgn-gda:DGN9add371cdf368b064d87a5eb4c340687 sio:SIO_000628 miriam-gene:4163 , lld:C0007129 ;
    a sio:SIO_001121 .
}
dgn-np:NP851639.RAeYMey7KUCmkUyULIlU3BV2aV-KPwfZHP5sxar7bw6iU130_provenance {
  dgn-np:NP851639.RAeYMey7KUCmkUyULIlU3BV2aV-KPwfZHP5sxar7bw6iU130_assertion dcterms:description "[We aimed to (a) highlight the risk of maternal cell contamination (MCC) in biochemical prenatal diagnosis, (b) establish the threshold of these biochemical assays to MCC, and (c) document the sensitivity of PCR based genotyping of microsatellites for the detection of MCC in prenatal diagnosis of inborn errors by biochemical analysis.]. 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:15635073 ;
    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:NP851639.RAeYMey7KUCmkUyULIlU3BV2aV-KPwfZHP5sxar7bw6iU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:40+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" .
}