@prefix semsc: <http://semanticscience.org/resource/> .
@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP209075.RACJIYDL6PpYqJdVjKH1naRcVR3Uo_r22KNDxxHsnqNwo> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@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 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:NP209075.RACJIYDL6PpYqJdVjKH1naRcVR3Uo_r22KNDxxHsnqNwo130_head {
  this: np:hasAssertion dgn-np:NP209075.RACJIYDL6PpYqJdVjKH1naRcVR3Uo_r22KNDxxHsnqNwo130_assertion;
    np:hasProvenance dgn-np:NP209075.RACJIYDL6PpYqJdVjKH1naRcVR3Uo_r22KNDxxHsnqNwo130_provenance;
    np:hasPublicationInfo dgn-np:NP209075.RACJIYDL6PpYqJdVjKH1naRcVR3Uo_r22KNDxxHsnqNwo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP209075.RACJIYDL6PpYqJdVjKH1naRcVR3Uo_r22KNDxxHsnqNwo130_assertion a np:Assertion .
  
  dgn-np:NP209075.RACJIYDL6PpYqJdVjKH1naRcVR3Uo_r22KNDxxHsnqNwo130_provenance a np:Provenance .
  
  dgn-np:NP209075.RACJIYDL6PpYqJdVjKH1naRcVR3Uo_r22KNDxxHsnqNwo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP209075.RACJIYDL6PpYqJdVjKH1naRcVR3Uo_r22KNDxxHsnqNwo130_assertion {
  miriam-gene:4000 a ncit:C16612 .
  
  lld:C0033300 a ncit:C7057 .
  
  dgn-gda:DGNab793f720d6e4f136d51855eb2852895 semsc:SIO_000628 miriam-gene:4000, lld:C0033300;
    a semsc:SIO_001121 .
}

dgn-np:NP209075.RACJIYDL6PpYqJdVjKH1naRcVR3Uo_r22KNDxxHsnqNwo130_provenance {
  dgn-np:NP209075.RACJIYDL6PpYqJdVjKH1naRcVR3Uo_r22KNDxxHsnqNwo130_assertion dct:description
      "[One of the major breakthroughs both in the lamin field and for this syndrome is that many of the cellular defects observed in HGPS patient cells and model systems can be restored after treatment with a class of compounds known as FTIs (farnesyltransferase inhibitors).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
    semsc:SIO_000772 miriam-pubmed:20074076;
    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:NP209075.RACJIYDL6PpYqJdVjKH1naRcVR3Uo_r22KNDxxHsnqNwo130_publicationInfo {
  this: dct:created "2014-10-02T12:33:55+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject semsc:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}