@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP196796.RAX3P95hggLuvMke3Cbx7Pjhqz2D-gzOdpy8MQyRf8n6k> .
@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:NP196796.RAX3P95hggLuvMke3Cbx7Pjhqz2D-gzOdpy8MQyRf8n6k130_head {
  this: np:hasAssertion dgn-np:NP196796.RAX3P95hggLuvMke3Cbx7Pjhqz2D-gzOdpy8MQyRf8n6k130_assertion;
    np:hasProvenance dgn-np:NP196796.RAX3P95hggLuvMke3Cbx7Pjhqz2D-gzOdpy8MQyRf8n6k130_provenance;
    np:hasPublicationInfo dgn-np:NP196796.RAX3P95hggLuvMke3Cbx7Pjhqz2D-gzOdpy8MQyRf8n6k130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP196796.RAX3P95hggLuvMke3Cbx7Pjhqz2D-gzOdpy8MQyRf8n6k130_assertion a np:Assertion .
  
  dgn-np:NP196796.RAX3P95hggLuvMke3Cbx7Pjhqz2D-gzOdpy8MQyRf8n6k130_provenance a np:Provenance .
  
  dgn-np:NP196796.RAX3P95hggLuvMke3Cbx7Pjhqz2D-gzOdpy8MQyRf8n6k130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP196796.RAX3P95hggLuvMke3Cbx7Pjhqz2D-gzOdpy8MQyRf8n6k130_assertion {
  miriam-gene:2263 a ncit:C16612 .
  
  lld:C0001193 a ncit:C7057 .
  
  dgn-gda:DGNd679c59c0e5d25545d11c0e5815e0418 sio:SIO_000628 miriam-gene:2263, lld:C0001193;
    a sio:SIO_001121 .
}

dgn-np:NP196796.RAX3P95hggLuvMke3Cbx7Pjhqz2D-gzOdpy8MQyRf8n6k130_provenance {
  dgn-np:NP196796.RAX3P95hggLuvMke3Cbx7Pjhqz2D-gzOdpy8MQyRf8n6k130_assertion dcterms:description
      "[The objective of this study was to determine whether there were any differences in the prevalence of ophthalmic features in Apert syndrome when comparing the Ser252Trp and Pro253Arg mutations in FGFR2.]. 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:17251833;
    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:NP196796.RAX3P95hggLuvMke3Cbx7Pjhqz2D-gzOdpy8MQyRf8n6k130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:48+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" .
}