@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP345230.RApt_pSChGkEpmWRHVl6eafqlbAWa-o_CXjEtpZDMBaUE> .
@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:NP345230.RApt_pSChGkEpmWRHVl6eafqlbAWa-o_CXjEtpZDMBaUE130_head {
  this: np:hasAssertion dgn-np:NP345230.RApt_pSChGkEpmWRHVl6eafqlbAWa-o_CXjEtpZDMBaUE130_assertion ;
    np:hasProvenance dgn-np:NP345230.RApt_pSChGkEpmWRHVl6eafqlbAWa-o_CXjEtpZDMBaUE130_provenance ;
    np:hasPublicationInfo dgn-np:NP345230.RApt_pSChGkEpmWRHVl6eafqlbAWa-o_CXjEtpZDMBaUE130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP345230.RApt_pSChGkEpmWRHVl6eafqlbAWa-o_CXjEtpZDMBaUE130_assertion a np:Assertion .
  dgn-np:NP345230.RApt_pSChGkEpmWRHVl6eafqlbAWa-o_CXjEtpZDMBaUE130_provenance a np:Provenance .
  dgn-np:NP345230.RApt_pSChGkEpmWRHVl6eafqlbAWa-o_CXjEtpZDMBaUE130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP345230.RApt_pSChGkEpmWRHVl6eafqlbAWa-o_CXjEtpZDMBaUE130_assertion {
  miriam-gene:1403 a ncit:C16612 .
  lld:C0265303 a ncit:C7057 .
  dgn-gda:DGN9875d92f59fe01a42efa0f3352948a1c sio:SIO_000628 miriam-gene:1403 , lld:C0265303 ;
    a sio:SIO_001121 .
}
dgn-np:NP345230.RApt_pSChGkEpmWRHVl6eafqlbAWa-o_CXjEtpZDMBaUE130_provenance {
  dgn-np:NP345230.RApt_pSChGkEpmWRHVl6eafqlbAWa-o_CXjEtpZDMBaUE130_assertion dcterms:description "[We present a case of Pfeiffer syndrome prenatally diagnosed at 20 weeks' gestation, in which the sonographic features of craniosynostosis, hypertelorism associated with an extreme proptosis, and broad thumb led to the diagnosis, confirmed after termination of pregnancy by dysmorphological, pathological and radiological evaluation.]. 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:15565658 ;
    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:NP345230.RApt_pSChGkEpmWRHVl6eafqlbAWa-o_CXjEtpZDMBaUE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:23+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" .
}