@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP560258.RAG5f3hL9wtiG3mpFos_EEdpTEkQDVsQmr1KikGGmoOPI> .
@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:NP560258.RAG5f3hL9wtiG3mpFos_EEdpTEkQDVsQmr1KikGGmoOPI130_head {
  this: np:hasAssertion dgn-np:NP560258.RAG5f3hL9wtiG3mpFos_EEdpTEkQDVsQmr1KikGGmoOPI130_assertion;
    np:hasProvenance dgn-np:NP560258.RAG5f3hL9wtiG3mpFos_EEdpTEkQDVsQmr1KikGGmoOPI130_provenance;
    np:hasPublicationInfo dgn-np:NP560258.RAG5f3hL9wtiG3mpFos_EEdpTEkQDVsQmr1KikGGmoOPI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP560258.RAG5f3hL9wtiG3mpFos_EEdpTEkQDVsQmr1KikGGmoOPI130_assertion a np:Assertion .
  
  dgn-np:NP560258.RAG5f3hL9wtiG3mpFos_EEdpTEkQDVsQmr1KikGGmoOPI130_provenance a np:Provenance .
  
  dgn-np:NP560258.RAG5f3hL9wtiG3mpFos_EEdpTEkQDVsQmr1KikGGmoOPI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP560258.RAG5f3hL9wtiG3mpFos_EEdpTEkQDVsQmr1KikGGmoOPI130_assertion {
  miriam-gene:7203 a ncit:C16612 .
  
  lld:C0025990 a ncit:C7057 .
  
  dgn-gda:DGNf92487d012742373305eba2174ec1d54 sio:SIO_000628 miriam-gene:7203, lld:C0025990;
    a sio:SIO_001121 .
}

dgn-np:NP560258.RAG5f3hL9wtiG3mpFos_EEdpTEkQDVsQmr1KikGGmoOPI130_provenance {
  dgn-np:NP560258.RAG5f3hL9wtiG3mpFos_EEdpTEkQDVsQmr1KikGGmoOPI130_assertion dcterms:description
      "[This comprehensive approach to expression profiling gives insights into the early development of the craniofacial region and provides markers for developmental structures and candidate genes, including SET and CCT3, for diseases such as orofacial clefting and micrognathia.]. 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:15703188;
    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:NP560258.RAG5f3hL9wtiG3mpFos_EEdpTEkQDVsQmr1KikGGmoOPI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:38+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" .
}