@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP537093.RAYXDQYXeDOD5VHBIvfVbChwVwJ4zLP4WeeXfK_vbbTMw> .
@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:NP537093.RAYXDQYXeDOD5VHBIvfVbChwVwJ4zLP4WeeXfK_vbbTMw130_head {
  this: np:hasAssertion dgn-np:NP537093.RAYXDQYXeDOD5VHBIvfVbChwVwJ4zLP4WeeXfK_vbbTMw130_assertion;
    np:hasProvenance dgn-np:NP537093.RAYXDQYXeDOD5VHBIvfVbChwVwJ4zLP4WeeXfK_vbbTMw130_provenance;
    np:hasPublicationInfo dgn-np:NP537093.RAYXDQYXeDOD5VHBIvfVbChwVwJ4zLP4WeeXfK_vbbTMw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP537093.RAYXDQYXeDOD5VHBIvfVbChwVwJ4zLP4WeeXfK_vbbTMw130_assertion a np:Assertion .
  
  dgn-np:NP537093.RAYXDQYXeDOD5VHBIvfVbChwVwJ4zLP4WeeXfK_vbbTMw130_provenance a np:Provenance .
  
  dgn-np:NP537093.RAYXDQYXeDOD5VHBIvfVbChwVwJ4zLP4WeeXfK_vbbTMw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP537093.RAYXDQYXeDOD5VHBIvfVbChwVwJ4zLP4WeeXfK_vbbTMw130_assertion {
  miriam-gene:4089 a ncit:C16612 .
  
  lld:C0039445 a ncit:C7057 .
  
  dgn-gda:DGN77a7ce634b6b7a3bb8560981d6f5f71b sio:SIO_000628 miriam-gene:4089, lld:C0039445;
    a sio:SIO_001121 .
}

dgn-np:NP537093.RAYXDQYXeDOD5VHBIvfVbChwVwJ4zLP4WeeXfK_vbbTMw130_provenance {
  dgn-np:NP537093.RAYXDQYXeDOD5VHBIvfVbChwVwJ4zLP4WeeXfK_vbbTMw130_assertion dcterms:description
      "[Patients with juvenile polyposis who have an MADH4 mutation should be screened for the vascular lesions associated with hereditary haemorrhagic telangiectasia, especially occult arteriovenous malformations in visceral organs that may otherwise present suddenly with serious medical consequences.]. 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:15031030;
    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:NP537093.RAYXDQYXeDOD5VHBIvfVbChwVwJ4zLP4WeeXfK_vbbTMw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:24+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" .
}