@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP607747.RAp_DIbiP11_KVGSEStmfhVQ7SXmGW-am7PZihMvTT_98> .
@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:NP607747.RAp_DIbiP11_KVGSEStmfhVQ7SXmGW-am7PZihMvTT_98130_head {
  this: np:hasAssertion dgn-np:NP607747.RAp_DIbiP11_KVGSEStmfhVQ7SXmGW-am7PZihMvTT_98130_assertion;
    np:hasProvenance dgn-np:NP607747.RAp_DIbiP11_KVGSEStmfhVQ7SXmGW-am7PZihMvTT_98130_provenance;
    np:hasPublicationInfo dgn-np:NP607747.RAp_DIbiP11_KVGSEStmfhVQ7SXmGW-am7PZihMvTT_98130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP607747.RAp_DIbiP11_KVGSEStmfhVQ7SXmGW-am7PZihMvTT_98130_assertion a np:Assertion .
  
  dgn-np:NP607747.RAp_DIbiP11_KVGSEStmfhVQ7SXmGW-am7PZihMvTT_98130_provenance a np:Provenance .
  
  dgn-np:NP607747.RAp_DIbiP11_KVGSEStmfhVQ7SXmGW-am7PZihMvTT_98130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP607747.RAp_DIbiP11_KVGSEStmfhVQ7SXmGW-am7PZihMvTT_98130_assertion {
  miriam-gene:25953 a ncit:C16612 .
  
  lld:C0020608 a ncit:C7057 .
  
  dgn-gda:DGN9ed8633de5650661dfe39fa0615230a1 sio:SIO_000628 miriam-gene:25953, lld:C0020608;
    a sio:SIO_001121 .
}

dgn-np:NP607747.RAp_DIbiP11_KVGSEStmfhVQ7SXmGW-am7PZihMvTT_98130_provenance {
  dgn-np:NP607747.RAp_DIbiP11_KVGSEStmfhVQ7SXmGW-am7PZihMvTT_98130_assertion dcterms:description
      "[Coupling these new clinical findings with results from recent molecular studies, we suggest that transcription factors such as MSX1 and PAX9, which have been associated with agenesis of molars, might be involved in the genetic control of Mn.I2.C transposition and PDC, tooth malpositions connected here with the specific expression of posterior-field (M3) hypodontia.]. 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:12490878;
    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:NP607747.RAp_DIbiP11_KVGSEStmfhVQ7SXmGW-am7PZihMvTT_98130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:04+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" .
}