@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP796884.RAKyothJSmLn2i3SnNVsiQF_7_xf9LH5o_lvka35IM2Gw> .
@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:NP796884.RAKyothJSmLn2i3SnNVsiQF_7_xf9LH5o_lvka35IM2Gw130_head {
  this: np:hasAssertion dgn-np:NP796884.RAKyothJSmLn2i3SnNVsiQF_7_xf9LH5o_lvka35IM2Gw130_assertion;
    np:hasProvenance dgn-np:NP796884.RAKyothJSmLn2i3SnNVsiQF_7_xf9LH5o_lvka35IM2Gw130_provenance;
    np:hasPublicationInfo dgn-np:NP796884.RAKyothJSmLn2i3SnNVsiQF_7_xf9LH5o_lvka35IM2Gw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP796884.RAKyothJSmLn2i3SnNVsiQF_7_xf9LH5o_lvka35IM2Gw130_assertion a np:Assertion .
  
  dgn-np:NP796884.RAKyothJSmLn2i3SnNVsiQF_7_xf9LH5o_lvka35IM2Gw130_provenance a np:Provenance .
  
  dgn-np:NP796884.RAKyothJSmLn2i3SnNVsiQF_7_xf9LH5o_lvka35IM2Gw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP796884.RAKyothJSmLn2i3SnNVsiQF_7_xf9LH5o_lvka35IM2Gw130_assertion {
  miriam-gene:258 a ncit:C16612 .
  
  lld:C0002452 a ncit:C7057 .
  
  dgn-gda:DGNf9ffa8c645cc06ade8719209b0dc87f5 sio:SIO_000628 miriam-gene:258, lld:C0002452;
    a sio:SIO_001121 .
}

dgn-np:NP796884.RAKyothJSmLn2i3SnNVsiQF_7_xf9LH5o_lvka35IM2Gw130_provenance {
  dgn-np:NP796884.RAKyothJSmLn2i3SnNVsiQF_7_xf9LH5o_lvka35IM2Gw130_assertion dcterms:description
      "[An identified human enamelin BAC genomic clone was shown to contain markers D4S2604 and D4S2670, as well as the first exon of the human ameloblastin gene, placing enamelin in the critical amelogenesis imperfecta locus between markers HIS1 and D4S2604 at 4q21.]. 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:11037750;
    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:NP796884.RAKyothJSmLn2i3SnNVsiQF_7_xf9LH5o_lvka35IM2Gw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:09+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" .
}