@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP683129.RAxWI30ugUvbEnh2CZWLmwyva_aL0NSWGARGzLlHpgNCU> .
@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:NP683129.RAxWI30ugUvbEnh2CZWLmwyva_aL0NSWGARGzLlHpgNCU130_head {
  this: np:hasAssertion dgn-np:NP683129.RAxWI30ugUvbEnh2CZWLmwyva_aL0NSWGARGzLlHpgNCU130_assertion;
    np:hasProvenance dgn-np:NP683129.RAxWI30ugUvbEnh2CZWLmwyva_aL0NSWGARGzLlHpgNCU130_provenance;
    np:hasPublicationInfo dgn-np:NP683129.RAxWI30ugUvbEnh2CZWLmwyva_aL0NSWGARGzLlHpgNCU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP683129.RAxWI30ugUvbEnh2CZWLmwyva_aL0NSWGARGzLlHpgNCU130_assertion a np:Assertion .
  
  dgn-np:NP683129.RAxWI30ugUvbEnh2CZWLmwyva_aL0NSWGARGzLlHpgNCU130_provenance a np:Provenance .
  
  dgn-np:NP683129.RAxWI30ugUvbEnh2CZWLmwyva_aL0NSWGARGzLlHpgNCU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP683129.RAxWI30ugUvbEnh2CZWLmwyva_aL0NSWGARGzLlHpgNCU130_assertion {
  miriam-gene:2737 a ncit:C16612 .
  
  lld:C0152427 a ncit:C7057 .
  
  dgn-gda:DGN4fd12cdead866e37891db2e3caf85aff sio:SIO_000628 miriam-gene:2737, lld:C0152427;
    a sio:SIO_001121 .
}

dgn-np:NP683129.RAxWI30ugUvbEnh2CZWLmwyva_aL0NSWGARGzLlHpgNCU130_provenance {
  dgn-np:NP683129.RAxWI30ugUvbEnh2CZWLmwyva_aL0NSWGARGzLlHpgNCU130_assertion dcterms:description
      "[Since FBXW11 is relatively highly expressed in fetal brain and is directly involved in proteolytic processing of GLI3, we propose FBXW11 as the most likely candidate gene for the HPE and prexial polydactyly 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:16865294;
    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:NP683129.RAxWI30ugUvbEnh2CZWLmwyva_aL0NSWGARGzLlHpgNCU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:55+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" .
}