@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP801256.RAGwnvhJcHyEsW2JqhYNVInYrxaVD06mQuXHd3bXpyMTY> .
@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:NP801256.RAGwnvhJcHyEsW2JqhYNVInYrxaVD06mQuXHd3bXpyMTY130_head {
  this: np:hasAssertion dgn-np:NP801256.RAGwnvhJcHyEsW2JqhYNVInYrxaVD06mQuXHd3bXpyMTY130_assertion;
    np:hasProvenance dgn-np:NP801256.RAGwnvhJcHyEsW2JqhYNVInYrxaVD06mQuXHd3bXpyMTY130_provenance;
    np:hasPublicationInfo dgn-np:NP801256.RAGwnvhJcHyEsW2JqhYNVInYrxaVD06mQuXHd3bXpyMTY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP801256.RAGwnvhJcHyEsW2JqhYNVInYrxaVD06mQuXHd3bXpyMTY130_assertion a np:Assertion .
  
  dgn-np:NP801256.RAGwnvhJcHyEsW2JqhYNVInYrxaVD06mQuXHd3bXpyMTY130_provenance a np:Provenance .
  
  dgn-np:NP801256.RAGwnvhJcHyEsW2JqhYNVInYrxaVD06mQuXHd3bXpyMTY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP801256.RAGwnvhJcHyEsW2JqhYNVInYrxaVD06mQuXHd3bXpyMTY130_assertion {
  miriam-gene:6469 a ncit:C16612 .
  
  lld:C0175694 a ncit:C7057 .
  
  dgn-gda:DGN725aa1671c9713051211d2fdc99eb6c4 sio:SIO_000628 miriam-gene:6469, lld:C0175694;
    a sio:SIO_001121 .
}

dgn-np:NP801256.RAGwnvhJcHyEsW2JqhYNVInYrxaVD06mQuXHd3bXpyMTY130_provenance {
  dgn-np:NP801256.RAGwnvhJcHyEsW2JqhYNVInYrxaVD06mQuXHd3bXpyMTY130_assertion dcterms:description
      "[When cholesterol was discovered to be the activator of sonic hedgehog, cholesterol deficiency with inactivation of this developmental patterning gene was thought to be the cause of SLOS malformations, yet this explanation is overly simplistic.]. 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:21777499;
    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:NP801256.RAGwnvhJcHyEsW2JqhYNVInYrxaVD06mQuXHd3bXpyMTY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:11+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" .
}