@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP526416.RAGbePGJqonPzrpsNs48ZqpNKX9DURIJUXjcYIhLLAyOQ> .
@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:NP526416.RAGbePGJqonPzrpsNs48ZqpNKX9DURIJUXjcYIhLLAyOQ130_head {
  this: np:hasAssertion dgn-np:NP526416.RAGbePGJqonPzrpsNs48ZqpNKX9DURIJUXjcYIhLLAyOQ130_assertion;
    np:hasProvenance dgn-np:NP526416.RAGbePGJqonPzrpsNs48ZqpNKX9DURIJUXjcYIhLLAyOQ130_provenance;
    np:hasPublicationInfo dgn-np:NP526416.RAGbePGJqonPzrpsNs48ZqpNKX9DURIJUXjcYIhLLAyOQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP526416.RAGbePGJqonPzrpsNs48ZqpNKX9DURIJUXjcYIhLLAyOQ130_assertion a np:Assertion .
  
  dgn-np:NP526416.RAGbePGJqonPzrpsNs48ZqpNKX9DURIJUXjcYIhLLAyOQ130_provenance a np:Provenance .
  
  dgn-np:NP526416.RAGbePGJqonPzrpsNs48ZqpNKX9DURIJUXjcYIhLLAyOQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP526416.RAGbePGJqonPzrpsNs48ZqpNKX9DURIJUXjcYIhLLAyOQ130_assertion {
  miriam-gene:2200 a ncit:C16612 .
  
  lld:C0024796 a ncit:C7057 .
  
  dgn-gda:DGN8555aeb43d83e243ef3e03906d6b7dec sio:SIO_000628 miriam-gene:2200, lld:C0024796;
    a sio:SIO_001121 .
}

dgn-np:NP526416.RAGbePGJqonPzrpsNs48ZqpNKX9DURIJUXjcYIhLLAyOQ130_provenance {
  dgn-np:NP526416.RAGbePGJqonPzrpsNs48ZqpNKX9DURIJUXjcYIhLLAyOQ130_assertion dcterms:description
      "[Genotype-phenotype correlation may contribute to anticipate the clinical consequences of specific FBN1 mutations more comprehensively and may be helpful to identify MFS patients at risk at on early stage of disease.]. 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:16342915;
    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:NP526416.RAGbePGJqonPzrpsNs48ZqpNKX9DURIJUXjcYIhLLAyOQ130_publicationInfo {
  this: dcterms:created "2016-05-13T12:45:43+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" .
}