@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP781630.RAyGpgh5Dz2gIHdHbcZ3cJqgTsDfGuX35VB48EReDauMM> .
@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/v4.0.0/void/> .

dgn-np:NP781630.RAyGpgh5Dz2gIHdHbcZ3cJqgTsDfGuX35VB48EReDauMM130_head {
  this: np:hasAssertion dgn-np:NP781630.RAyGpgh5Dz2gIHdHbcZ3cJqgTsDfGuX35VB48EReDauMM130_assertion;
    np:hasProvenance dgn-np:NP781630.RAyGpgh5Dz2gIHdHbcZ3cJqgTsDfGuX35VB48EReDauMM130_provenance;
    np:hasPublicationInfo dgn-np:NP781630.RAyGpgh5Dz2gIHdHbcZ3cJqgTsDfGuX35VB48EReDauMM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP781630.RAyGpgh5Dz2gIHdHbcZ3cJqgTsDfGuX35VB48EReDauMM130_assertion a np:Assertion .
  
  dgn-np:NP781630.RAyGpgh5Dz2gIHdHbcZ3cJqgTsDfGuX35VB48EReDauMM130_provenance a np:Provenance .
  
  dgn-np:NP781630.RAyGpgh5Dz2gIHdHbcZ3cJqgTsDfGuX35VB48EReDauMM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP781630.RAyGpgh5Dz2gIHdHbcZ3cJqgTsDfGuX35VB48EReDauMM130_assertion {
  miriam-gene:10117 a ncit:C16612 .
  
  lld:C0002452 a ncit:C7057 .
  
  dgn-gda:DGN54e5fec669a0121dc3b491e2729bddaa sio:SIO_000628 miriam-gene:10117, lld:C0002452;
    a sio:SIO_001121 .
}

dgn-np:NP781630.RAyGpgh5Dz2gIHdHbcZ3cJqgTsDfGuX35VB48EReDauMM130_provenance {
  dgn-np:NP781630.RAyGpgh5Dz2gIHdHbcZ3cJqgTsDfGuX35VB48EReDauMM130_assertion dcterms:description
      "[Taken together, these findings improve our understanding of ENAM evolution and provide new information that would be useful for further investigation of ENAM function as well as for the validation of mutations leading to amelogenesis imperfecta.]. 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:20012271;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP781630.RAyGpgh5Dz2gIHdHbcZ3cJqgTsDfGuX35VB48EReDauMM130_publicationInfo {
  this: dcterms:created "2016-05-13T12:47:39+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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}