@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP202900.RAUwlwpgErxW7lNNuoPY2V2JuzESmMOOwnKARn3DuXuMU> .
@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:NP202900.RAUwlwpgErxW7lNNuoPY2V2JuzESmMOOwnKARn3DuXuMU130_head {
  this: np:hasAssertion dgn-np:NP202900.RAUwlwpgErxW7lNNuoPY2V2JuzESmMOOwnKARn3DuXuMU130_assertion;
    np:hasProvenance dgn-np:NP202900.RAUwlwpgErxW7lNNuoPY2V2JuzESmMOOwnKARn3DuXuMU130_provenance;
    np:hasPublicationInfo dgn-np:NP202900.RAUwlwpgErxW7lNNuoPY2V2JuzESmMOOwnKARn3DuXuMU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP202900.RAUwlwpgErxW7lNNuoPY2V2JuzESmMOOwnKARn3DuXuMU130_assertion a np:Assertion .
  
  dgn-np:NP202900.RAUwlwpgErxW7lNNuoPY2V2JuzESmMOOwnKARn3DuXuMU130_provenance a np:Provenance .
  
  dgn-np:NP202900.RAUwlwpgErxW7lNNuoPY2V2JuzESmMOOwnKARn3DuXuMU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP202900.RAUwlwpgErxW7lNNuoPY2V2JuzESmMOOwnKARn3DuXuMU130_assertion {
  miriam-gene:324 a ncit:C16612 .
  
  lld:C0033036 a ncit:C7057 .
  
  dgn-gda:DGN66ff36c6acf3d716fa996b8cdb1790ae sio:SIO_000628 miriam-gene:324, lld:C0033036;
    a sio:SIO_001121 .
}

dgn-np:NP202900.RAUwlwpgErxW7lNNuoPY2V2JuzESmMOOwnKARn3DuXuMU130_provenance {
  dgn-np:NP202900.RAUwlwpgErxW7lNNuoPY2V2JuzESmMOOwnKARn3DuXuMU130_assertion dcterms:description
      "[Of more immediate clinical interest is the observation that specific APC mutations appear to participate in the severity of the disease and determine the development of hypertrophy of the retinal pigment epithelium, a diagnostically important manifestation of the APC disease found in 70% of the patients.]. 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:7675542;
    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:NP202900.RAUwlwpgErxW7lNNuoPY2V2JuzESmMOOwnKARn3DuXuMU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:52+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" .
}