@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP440102.RAzR_yQqQWFuTXoPIfUn3NTZRmXPvWH8mSu3CNgMbHQ_8> .
@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:NP440102.RAzR_yQqQWFuTXoPIfUn3NTZRmXPvWH8mSu3CNgMbHQ_8130_head {
  this: np:hasAssertion dgn-np:NP440102.RAzR_yQqQWFuTXoPIfUn3NTZRmXPvWH8mSu3CNgMbHQ_8130_assertion;
    np:hasProvenance dgn-np:NP440102.RAzR_yQqQWFuTXoPIfUn3NTZRmXPvWH8mSu3CNgMbHQ_8130_provenance;
    np:hasPublicationInfo dgn-np:NP440102.RAzR_yQqQWFuTXoPIfUn3NTZRmXPvWH8mSu3CNgMbHQ_8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP440102.RAzR_yQqQWFuTXoPIfUn3NTZRmXPvWH8mSu3CNgMbHQ_8130_assertion a np:Assertion .
  
  dgn-np:NP440102.RAzR_yQqQWFuTXoPIfUn3NTZRmXPvWH8mSu3CNgMbHQ_8130_provenance a np:Provenance .
  
  dgn-np:NP440102.RAzR_yQqQWFuTXoPIfUn3NTZRmXPvWH8mSu3CNgMbHQ_8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP440102.RAzR_yQqQWFuTXoPIfUn3NTZRmXPvWH8mSu3CNgMbHQ_8130_assertion {
  miriam-gene:1540 a ncit:C16612 .
  
  lld:C1305968 a ncit:C7057 .
  
  dgn-gda:DGNa4fbdda9df19bbf2f3901ee14ed84ee1 sio:SIO_000628 miriam-gene:1540, lld:C1305968;
    a sio:SIO_001121 .
}

dgn-np:NP440102.RAzR_yQqQWFuTXoPIfUn3NTZRmXPvWH8mSu3CNgMbHQ_8130_provenance {
  dgn-np:NP440102.RAzR_yQqQWFuTXoPIfUn3NTZRmXPvWH8mSu3CNgMbHQ_8130_assertion dcterms:description
      "[The study firstly identified the cylindromatosis gene responsible for MFT and showed that different mutations of the CYLDI gene can give rise to distinct clinical and histological expression such as FC and MFT.]. 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:15086550;
    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:NP440102.RAzR_yQqQWFuTXoPIfUn3NTZRmXPvWH8mSu3CNgMbHQ_8130_publicationInfo {
  this: dcterms:created "2016-05-13T12:45:04+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" .
}