@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP525367.RAbfh_rqqHo4sJmF5hzKbbwADNuxNdy-MGYx8ZDPR4HGU> .
@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:NP525367.RAbfh_rqqHo4sJmF5hzKbbwADNuxNdy-MGYx8ZDPR4HGU130_head {
  this: np:hasAssertion dgn-np:NP525367.RAbfh_rqqHo4sJmF5hzKbbwADNuxNdy-MGYx8ZDPR4HGU130_assertion;
    np:hasProvenance dgn-np:NP525367.RAbfh_rqqHo4sJmF5hzKbbwADNuxNdy-MGYx8ZDPR4HGU130_provenance;
    np:hasPublicationInfo dgn-np:NP525367.RAbfh_rqqHo4sJmF5hzKbbwADNuxNdy-MGYx8ZDPR4HGU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP525367.RAbfh_rqqHo4sJmF5hzKbbwADNuxNdy-MGYx8ZDPR4HGU130_assertion a np:Assertion .
  
  dgn-np:NP525367.RAbfh_rqqHo4sJmF5hzKbbwADNuxNdy-MGYx8ZDPR4HGU130_provenance a np:Provenance .
  
  dgn-np:NP525367.RAbfh_rqqHo4sJmF5hzKbbwADNuxNdy-MGYx8ZDPR4HGU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP525367.RAbfh_rqqHo4sJmF5hzKbbwADNuxNdy-MGYx8ZDPR4HGU130_assertion {
  miriam-gene:3714 a ncit:C16612 .
  
  lld:C0810364 a ncit:C7057 .
  
  dgn-gda:DGNce237907013745c1791846fa3fa9de96 sio:SIO_000628 miriam-gene:3714, lld:C0810364;
    a sio:SIO_001121 .
}

dgn-np:NP525367.RAbfh_rqqHo4sJmF5hzKbbwADNuxNdy-MGYx8ZDPR4HGU130_provenance {
  dgn-np:NP525367.RAbfh_rqqHo4sJmF5hzKbbwADNuxNdy-MGYx8ZDPR4HGU130_assertion dcterms:description
      "[Sequence analysis alone suggests that point mutations in FOXE1, GLI2, JAG2, LHX8, MSX1, MSX2, SATB2, SKI, SPRY2, and TBX10 may be rare causes of isolated cleft lip with or without cleft palate, and the linkage disequilibrium data support a larger, as yet unspecified, role for variants in or near MSX2, JAG2, and SKI.]. 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:16327884;
    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:NP525367.RAbfh_rqqHo4sJmF5hzKbbwADNuxNdy-MGYx8ZDPR4HGU130_publicationInfo {
  this: dcterms:created "2016-05-13T12:45:43+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" .
}