@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP493741.RAaQc8Mt2f1QWW4A9HFK0e1LfLDQ49E0qqlak0mx0UmAg> .
@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:NP493741.RAaQc8Mt2f1QWW4A9HFK0e1LfLDQ49E0qqlak0mx0UmAg130_head {
  this: np:hasAssertion dgn-np:NP493741.RAaQc8Mt2f1QWW4A9HFK0e1LfLDQ49E0qqlak0mx0UmAg130_assertion;
    np:hasProvenance dgn-np:NP493741.RAaQc8Mt2f1QWW4A9HFK0e1LfLDQ49E0qqlak0mx0UmAg130_provenance;
    np:hasPublicationInfo dgn-np:NP493741.RAaQc8Mt2f1QWW4A9HFK0e1LfLDQ49E0qqlak0mx0UmAg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP493741.RAaQc8Mt2f1QWW4A9HFK0e1LfLDQ49E0qqlak0mx0UmAg130_assertion a np:Assertion .
  
  dgn-np:NP493741.RAaQc8Mt2f1QWW4A9HFK0e1LfLDQ49E0qqlak0mx0UmAg130_provenance a np:Provenance .
  
  dgn-np:NP493741.RAaQc8Mt2f1QWW4A9HFK0e1LfLDQ49E0qqlak0mx0UmAg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP493741.RAaQc8Mt2f1QWW4A9HFK0e1LfLDQ49E0qqlak0mx0UmAg130_assertion {
  miriam-gene:2521 a ncit:C16612 .
  
  lld:C0016412 a ncit:C7057 .
  
  dgn-gda:DGNf5456e21031a6eaea18a26ec4b30f322 sio:SIO_000628 miriam-gene:2521, lld:C0016412;
    a sio:SIO_001121 .
}

dgn-np:NP493741.RAaQc8Mt2f1QWW4A9HFK0e1LfLDQ49E0qqlak0mx0UmAg130_provenance {
  dgn-np:NP493741.RAaQc8Mt2f1QWW4A9HFK0e1LfLDQ49E0qqlak0mx0UmAg130_assertion dcterms:description
      "[It was concluded that the FUS, CIR, and HS morphologies represent promising biomarkers of CIN that are sensitive to folate deficiency, and further validation and investigation of the mechanisms responsible for their formation is warranted.]. 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:22430981;
    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:NP493741.RAaQc8Mt2f1QWW4A9HFK0e1LfLDQ49E0qqlak0mx0UmAg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:55+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: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" .
}