@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP705335.RAOpNyoBBpRBS2xZ2SgFWLfplQWujCXW3U4d3N461mNIo> .
@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:NP705335.RAOpNyoBBpRBS2xZ2SgFWLfplQWujCXW3U4d3N461mNIo130_head {
  this: np:hasAssertion dgn-np:NP705335.RAOpNyoBBpRBS2xZ2SgFWLfplQWujCXW3U4d3N461mNIo130_assertion;
    np:hasProvenance dgn-np:NP705335.RAOpNyoBBpRBS2xZ2SgFWLfplQWujCXW3U4d3N461mNIo130_provenance;
    np:hasPublicationInfo dgn-np:NP705335.RAOpNyoBBpRBS2xZ2SgFWLfplQWujCXW3U4d3N461mNIo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP705335.RAOpNyoBBpRBS2xZ2SgFWLfplQWujCXW3U4d3N461mNIo130_assertion a np:Assertion .
  
  dgn-np:NP705335.RAOpNyoBBpRBS2xZ2SgFWLfplQWujCXW3U4d3N461mNIo130_provenance a np:Provenance .
  
  dgn-np:NP705335.RAOpNyoBBpRBS2xZ2SgFWLfplQWujCXW3U4d3N461mNIo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP705335.RAOpNyoBBpRBS2xZ2SgFWLfplQWujCXW3U4d3N461mNIo130_assertion {
  miriam-gene:4016 a ncit:C16612 .
  
  lld:C0206368 a ncit:C7057 .
  
  dgn-gda:DGN9147f38f4869455bfe79e383f3b38591 sio:SIO_000628 miriam-gene:4016, lld:C0206368;
    a sio:SIO_001121 .
}

dgn-np:NP705335.RAOpNyoBBpRBS2xZ2SgFWLfplQWujCXW3U4d3N461mNIo130_provenance {
  dgn-np:NP705335.RAOpNyoBBpRBS2xZ2SgFWLfplQWujCXW3U4d3N461mNIo130_assertion dcterms:description
      "[Recent human genetic association studies have identified changes occurring in the LOXL1 gene as an important risk factor for XFS but also indicated that other factors contributing to risk likely exist.]. 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:19029039;
    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:NP705335.RAOpNyoBBpRBS2xZ2SgFWLfplQWujCXW3U4d3N461mNIo130_publicationInfo {
  this: dcterms:created "2016-05-13T12:47:04+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" .
}