@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP198112.RApN1z-2xJMnAOBMjjwXNtuTfR1XspI_LWKitJlWXQ33c> .
@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:NP198112.RApN1z-2xJMnAOBMjjwXNtuTfR1XspI_LWKitJlWXQ33c130_head {
  this: np:hasAssertion dgn-np:NP198112.RApN1z-2xJMnAOBMjjwXNtuTfR1XspI_LWKitJlWXQ33c130_assertion ;
    np:hasProvenance dgn-np:NP198112.RApN1z-2xJMnAOBMjjwXNtuTfR1XspI_LWKitJlWXQ33c130_provenance ;
    np:hasPublicationInfo dgn-np:NP198112.RApN1z-2xJMnAOBMjjwXNtuTfR1XspI_LWKitJlWXQ33c130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP198112.RApN1z-2xJMnAOBMjjwXNtuTfR1XspI_LWKitJlWXQ33c130_assertion a np:Assertion .
  dgn-np:NP198112.RApN1z-2xJMnAOBMjjwXNtuTfR1XspI_LWKitJlWXQ33c130_provenance a np:Provenance .
  dgn-np:NP198112.RApN1z-2xJMnAOBMjjwXNtuTfR1XspI_LWKitJlWXQ33c130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP198112.RApN1z-2xJMnAOBMjjwXNtuTfR1XspI_LWKitJlWXQ33c130_assertion {
  miriam-gene:7291 a ncit:C16612 .
  lld:C0265303 a ncit:C7057 .
  dgn-gda:DGNed262879b6dfb43f483c52c4e267daa1 sio:SIO_000628 miriam-gene:7291 , lld:C0265303 ;
    a sio:SIO_001121 .
}
dgn-np:NP198112.RApN1z-2xJMnAOBMjjwXNtuTfR1XspI_LWKitJlWXQ33c130_provenance {
  dgn-np:NP198112.RApN1z-2xJMnAOBMjjwXNtuTfR1XspI_LWKitJlWXQ33c130_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:NP198112.RApN1z-2xJMnAOBMjjwXNtuTfR1XspI_LWKitJlWXQ33c130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:49+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" .
}