@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP145877.RAoGKB3Y5NRXgFYnUGeSVTXJgrZmYkdLzGrwOjpVftZCc> .
@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:NP145877.RAoGKB3Y5NRXgFYnUGeSVTXJgrZmYkdLzGrwOjpVftZCc130_head {
  this: np:hasAssertion dgn-np:NP145877.RAoGKB3Y5NRXgFYnUGeSVTXJgrZmYkdLzGrwOjpVftZCc130_assertion;
    np:hasProvenance dgn-np:NP145877.RAoGKB3Y5NRXgFYnUGeSVTXJgrZmYkdLzGrwOjpVftZCc130_provenance;
    np:hasPublicationInfo dgn-np:NP145877.RAoGKB3Y5NRXgFYnUGeSVTXJgrZmYkdLzGrwOjpVftZCc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP145877.RAoGKB3Y5NRXgFYnUGeSVTXJgrZmYkdLzGrwOjpVftZCc130_assertion a np:Assertion .
  
  dgn-np:NP145877.RAoGKB3Y5NRXgFYnUGeSVTXJgrZmYkdLzGrwOjpVftZCc130_provenance a np:Provenance .
  
  dgn-np:NP145877.RAoGKB3Y5NRXgFYnUGeSVTXJgrZmYkdLzGrwOjpVftZCc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP145877.RAoGKB3Y5NRXgFYnUGeSVTXJgrZmYkdLzGrwOjpVftZCc130_assertion {
  miriam-gene:2248 a ncit:C16612 .
  
  lld:C0581883 a ncit:C7057 .
  
  dgn-gda:DGN79ca4286b496f6d03b23fab0a0dad469 sio:SIO_000628 miriam-gene:2248, lld:C0581883;
    a sio:SIO_001121 .
}

dgn-np:NP145877.RAoGKB3Y5NRXgFYnUGeSVTXJgrZmYkdLzGrwOjpVftZCc130_provenance {
  dgn-np:NP145877.RAoGKB3Y5NRXgFYnUGeSVTXJgrZmYkdLzGrwOjpVftZCc130_assertion dcterms:description
      "[sequenced the FGF3 gene in 10 unrelated families in which probands had congenital deafness associated with various inner ear anomalies, including Michel aplasia, with or without tooth or external ear anomalies.]. 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:18435799;
    prov:wasDerivedFrom dgn-void:lhgdn-20090331;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:lhgdn-20090331 pav:importedOn "2009-03-31"^^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:NP145877.RAoGKB3Y5NRXgFYnUGeSVTXJgrZmYkdLzGrwOjpVftZCc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:16+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" .
}