@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP625126.RA_69-z_3YcLlUO0pWpT7CpgEGGOdQFJAHuMs5p2XN3uY> .
@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:NP625126.RA_69-z_3YcLlUO0pWpT7CpgEGGOdQFJAHuMs5p2XN3uY130_head {
   this: np:hasAssertion dgn-np:NP625126.RA_69-z_3YcLlUO0pWpT7CpgEGGOdQFJAHuMs5p2XN3uY130_assertion ;
    np:hasProvenance dgn-np:NP625126.RA_69-z_3YcLlUO0pWpT7CpgEGGOdQFJAHuMs5p2XN3uY130_provenance ;
    np:hasPublicationInfo dgn-np:NP625126.RA_69-z_3YcLlUO0pWpT7CpgEGGOdQFJAHuMs5p2XN3uY130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP625126.RA_69-z_3YcLlUO0pWpT7CpgEGGOdQFJAHuMs5p2XN3uY130_assertion a np:Assertion .
  dgn-np:NP625126.RA_69-z_3YcLlUO0pWpT7CpgEGGOdQFJAHuMs5p2XN3uY130_provenance a np:Provenance .
  dgn-np:NP625126.RA_69-z_3YcLlUO0pWpT7CpgEGGOdQFJAHuMs5p2XN3uY130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP625126.RA_69-z_3YcLlUO0pWpT7CpgEGGOdQFJAHuMs5p2XN3uY130_assertion {
   miriam-gene:57216 a ncit:C16612 .
  lld:C0025990 a ncit:C7057 .
  dgn-gda:DGN317f03f681fad56085e7cb99a14459e3 sio:SIO_000628 miriam-gene:57216 , lld:C0025990 ;
    a sio:SIO_001121 .
}
dgn-np:NP625126.RA_69-z_3YcLlUO0pWpT7CpgEGGOdQFJAHuMs5p2XN3uY130_provenance {
   dgn-np:NP625126.RA_69-z_3YcLlUO0pWpT7CpgEGGOdQFJAHuMs5p2XN3uY130_assertion dcterms:description "[Other alterations frequently observed are decreased biparietal diameter, hypertelorism, hypotelorism, absent eyebrows, prominent eyes with ptosis, receding chin, dysmorphic ears, large extremities, prominent nasal bridge, long philtrum, epicthus, strabismus, and micrognathia (3-5).]. 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:19106480 ;
    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:NP625126.RA_69-z_3YcLlUO0pWpT7CpgEGGOdQFJAHuMs5p2XN3uY130_publicationInfo {
   this: dcterms:created "2014-10-02T12:38:17+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" .
}