@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP702896.RAzExlwZ3vWRNzcIw_q9XpT3Q_9MvgwkQnH0ViECsrrKI> .
@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:NP702896.RAzExlwZ3vWRNzcIw_q9XpT3Q_9MvgwkQnH0ViECsrrKI130_head {
  this: np:hasAssertion dgn-np:NP702896.RAzExlwZ3vWRNzcIw_q9XpT3Q_9MvgwkQnH0ViECsrrKI130_assertion ;
    np:hasProvenance dgn-np:NP702896.RAzExlwZ3vWRNzcIw_q9XpT3Q_9MvgwkQnH0ViECsrrKI130_provenance ;
    np:hasPublicationInfo dgn-np:NP702896.RAzExlwZ3vWRNzcIw_q9XpT3Q_9MvgwkQnH0ViECsrrKI130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP702896.RAzExlwZ3vWRNzcIw_q9XpT3Q_9MvgwkQnH0ViECsrrKI130_assertion a np:Assertion .
  dgn-np:NP702896.RAzExlwZ3vWRNzcIw_q9XpT3Q_9MvgwkQnH0ViECsrrKI130_provenance a np:Provenance .
  dgn-np:NP702896.RAzExlwZ3vWRNzcIw_q9XpT3Q_9MvgwkQnH0ViECsrrKI130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP702896.RAzExlwZ3vWRNzcIw_q9XpT3Q_9MvgwkQnH0ViECsrrKI130_assertion {
  miriam-gene:2001 a ncit:C16612 .
  lld:C0013537 a ncit:C7057 .
  dgn-gda:DGN6a869cd911f05381555048011e41696a sio:SIO_000628 miriam-gene:2001 , lld:C0013537 ;
    a sio:SIO_001121 .
}
dgn-np:NP702896.RAzExlwZ3vWRNzcIw_q9XpT3Q_9MvgwkQnH0ViECsrrKI130_provenance {
  dgn-np:NP702896.RAzExlwZ3vWRNzcIw_q9XpT3Q_9MvgwkQnH0ViECsrrKI130_assertion dcterms:description "[Our identification of the trophoblast-specific transcriptional circuit established by ELF5 will be instrumental to derive human TS cell lines that truly reflect early placental trophoblast and that will be most beneficial to gain insights into the aetiology of common pregnancy complications, including intra-uterine growth restriction and pre-eclampsia.]. 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:20354077 ;
    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:NP702896.RAzExlwZ3vWRNzcIw_q9XpT3Q_9MvgwkQnH0ViECsrrKI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:07+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> ;
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}