@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP397034.RA4-d8sjIPam7fkOBgWEdjk9Fntq5myjIKn7__5TFTeOE> .
@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:NP397034.RA4-d8sjIPam7fkOBgWEdjk9Fntq5myjIKn7__5TFTeOE130_head {
  this: np:hasAssertion dgn-np:NP397034.RA4-d8sjIPam7fkOBgWEdjk9Fntq5myjIKn7__5TFTeOE130_assertion;
    np:hasProvenance dgn-np:NP397034.RA4-d8sjIPam7fkOBgWEdjk9Fntq5myjIKn7__5TFTeOE130_provenance;
    np:hasPublicationInfo dgn-np:NP397034.RA4-d8sjIPam7fkOBgWEdjk9Fntq5myjIKn7__5TFTeOE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP397034.RA4-d8sjIPam7fkOBgWEdjk9Fntq5myjIKn7__5TFTeOE130_assertion a np:Assertion .
  
  dgn-np:NP397034.RA4-d8sjIPam7fkOBgWEdjk9Fntq5myjIKn7__5TFTeOE130_provenance a np:Provenance .
  
  dgn-np:NP397034.RA4-d8sjIPam7fkOBgWEdjk9Fntq5myjIKn7__5TFTeOE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP397034.RA4-d8sjIPam7fkOBgWEdjk9Fntq5myjIKn7__5TFTeOE130_assertion {
  miriam-gene:860 a ncit:C16612 .
  
  lld:C2699510 a ncit:C7057 .
  
  dgn-gda:DGN7ae8ce9ec1d21b064f1bc7ad018ea867 sio:SIO_000628 miriam-gene:860, lld:C2699510;
    a sio:SIO_001121 .
}

dgn-np:NP397034.RA4-d8sjIPam7fkOBgWEdjk9Fntq5myjIKn7__5TFTeOE130_provenance {
  dgn-np:NP397034.RA4-d8sjIPam7fkOBgWEdjk9Fntq5myjIKn7__5TFTeOE130_assertion dcterms:description
      "[These p63alpha mutations also affected the transcriptional regulation of gene targets involved in bone and tooth development (e.g., RUNX2 and MINT) and therefore might contribute to the molecular mechanisms underlying the SHFM phenotype.]. 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:15539951;
    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:NP397034.RA4-d8sjIPam7fkOBgWEdjk9Fntq5myjIKn7__5TFTeOE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:56+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" .
}