@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP339101.RAwXB0FOmCbEF2dVm1wwJgBhrfmzsIR54I0WAgrR57rs8> .
@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/v3.0.0/void/> .

dgn-np:NP339101.RAwXB0FOmCbEF2dVm1wwJgBhrfmzsIR54I0WAgrR57rs8130_head {
  this: np:hasAssertion dgn-np:NP339101.RAwXB0FOmCbEF2dVm1wwJgBhrfmzsIR54I0WAgrR57rs8130_assertion;
    np:hasProvenance dgn-np:NP339101.RAwXB0FOmCbEF2dVm1wwJgBhrfmzsIR54I0WAgrR57rs8130_provenance;
    np:hasPublicationInfo dgn-np:NP339101.RAwXB0FOmCbEF2dVm1wwJgBhrfmzsIR54I0WAgrR57rs8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP339101.RAwXB0FOmCbEF2dVm1wwJgBhrfmzsIR54I0WAgrR57rs8130_assertion a np:Assertion .
  
  dgn-np:NP339101.RAwXB0FOmCbEF2dVm1wwJgBhrfmzsIR54I0WAgrR57rs8130_provenance a np:Provenance .
  
  dgn-np:NP339101.RAwXB0FOmCbEF2dVm1wwJgBhrfmzsIR54I0WAgrR57rs8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP339101.RAwXB0FOmCbEF2dVm1wwJgBhrfmzsIR54I0WAgrR57rs8130_assertion {
  miriam-gene:1540 a ncit:C16612 .
  
  lld:C1275122 a ncit:C7057 .
  
  dgn-gda:DGNe6ae5f4851fe47df3691d2dbaf78bfc2 sio:SIO_000628 miriam-gene:1540, lld:C1275122;
    a sio:SIO_001122 .
}

dgn-np:NP339101.RAwXB0FOmCbEF2dVm1wwJgBhrfmzsIR54I0WAgrR57rs8130_provenance {
  dgn-np:NP339101.RAwXB0FOmCbEF2dVm1wwJgBhrfmzsIR54I0WAgrR57rs8130_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-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP339101.RAwXB0FOmCbEF2dVm1wwJgBhrfmzsIR54I0WAgrR57rs8130_publicationInfo {
  this: dcterms:created "2015-08-25T14:40:55+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: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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}