@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP949003.RAxIveuPF2MBFYw8RVBZdXbBpVwd61qmilSDHMQ_F1yLM> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP949003.RAxIveuPF2MBFYw8RVBZdXbBpVwd61qmilSDHMQ_F1yLM130_head {
  this: np:hasAssertion dgn-np:NP949003.RAxIveuPF2MBFYw8RVBZdXbBpVwd61qmilSDHMQ_F1yLM130_assertion;
    np:hasProvenance dgn-np:NP949003.RAxIveuPF2MBFYw8RVBZdXbBpVwd61qmilSDHMQ_F1yLM130_provenance;
    np:hasPublicationInfo dgn-np:NP949003.RAxIveuPF2MBFYw8RVBZdXbBpVwd61qmilSDHMQ_F1yLM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP949003.RAxIveuPF2MBFYw8RVBZdXbBpVwd61qmilSDHMQ_F1yLM130_assertion a np:Assertion .
  
  dgn-np:NP949003.RAxIveuPF2MBFYw8RVBZdXbBpVwd61qmilSDHMQ_F1yLM130_provenance a np:Provenance .
  
  dgn-np:NP949003.RAxIveuPF2MBFYw8RVBZdXbBpVwd61qmilSDHMQ_F1yLM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP949003.RAxIveuPF2MBFYw8RVBZdXbBpVwd61qmilSDHMQ_F1yLM130_assertion {
  miriam-gene:80326 a ncit:C16612 .
  
  lld:C0700590 a ncit:C7057 .
  
  dgn-gda:DGN831c4721c1d21e263467ff679b9a5fec sio:SIO_000628 miriam-gene:80326, lld:C0700590;
    a sio:SIO_001121 .
}

dgn-np:NP949003.RAxIveuPF2MBFYw8RVBZdXbBpVwd61qmilSDHMQ_F1yLM130_provenance {
  dgn-np:NP949003.RAxIveuPF2MBFYw8RVBZdXbBpVwd61qmilSDHMQ_F1yLM130_assertion dcterms:description
      "[OODD is a rare form of autosomal recessive ectodermal dysplasia involving hair, teeth, nails, and skin, characterized by hypodontia (tooth agenesis), smooth tongue with marked reduction of filiform and fungiform papillae, nail dysplasia, dry skin, palmoplantar keratoderma, and hyperhidrosis of palms and soles.]. 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:24458874;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP949003.RAxIveuPF2MBFYw8RVBZdXbBpVwd61qmilSDHMQ_F1yLM130_publicationInfo {
  this: dcterms:created "2015-08-25T14:47:19+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}