@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP210352.RAsGceTI4QONVMp-7a1sVSunR5qYUXuPi3w_sYz41_ZGg> .
@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:NP210352.RAsGceTI4QONVMp-7a1sVSunR5qYUXuPi3w_sYz41_ZGg130_head {
  this: np:hasAssertion dgn-np:NP210352.RAsGceTI4QONVMp-7a1sVSunR5qYUXuPi3w_sYz41_ZGg130_assertion;
    np:hasProvenance dgn-np:NP210352.RAsGceTI4QONVMp-7a1sVSunR5qYUXuPi3w_sYz41_ZGg130_provenance;
    np:hasPublicationInfo dgn-np:NP210352.RAsGceTI4QONVMp-7a1sVSunR5qYUXuPi3w_sYz41_ZGg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP210352.RAsGceTI4QONVMp-7a1sVSunR5qYUXuPi3w_sYz41_ZGg130_assertion a np:Assertion .
  
  dgn-np:NP210352.RAsGceTI4QONVMp-7a1sVSunR5qYUXuPi3w_sYz41_ZGg130_provenance a np:Provenance .
  
  dgn-np:NP210352.RAsGceTI4QONVMp-7a1sVSunR5qYUXuPi3w_sYz41_ZGg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP210352.RAsGceTI4QONVMp-7a1sVSunR5qYUXuPi3w_sYz41_ZGg130_assertion {
  miriam-gene:999 a ncit:C16612 .
  
  lld:C0678222 a ncit:C7057 .
  
  dgn-gda:DGNd31727be065d00a0aa2702e040befd2d sio:SIO_000628 miriam-gene:999, lld:C0678222;
    a sio:SIO_001121 .
}

dgn-np:NP210352.RAsGceTI4QONVMp-7a1sVSunR5qYUXuPi3w_sYz41_ZGg130_provenance {
  dgn-np:NP210352.RAsGceTI4QONVMp-7a1sVSunR5qYUXuPi3w_sYz41_ZGg130_assertion dcterms:description
      "[Areas for future research are discussed, including development of new screening modalities, optimal timing of prophylactic gastrectomy, identification of additional causative mutations in HDGC, management of patients with CDH1 missense mutations and prevention/early detection of lobular breast cancer in CDH1 mutation carriers.]. 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:18684065;
    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:NP210352.RAsGceTI4QONVMp-7a1sVSunR5qYUXuPi3w_sYz41_ZGg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:56+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" .
}