@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1275020.RAljn9oegsWvUnEtjDeDopwON3FcO2E9Q9drNJEOlWRfw> .
@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:NP1275020.RAljn9oegsWvUnEtjDeDopwON3FcO2E9Q9drNJEOlWRfw130_head {
  this: np:hasAssertion dgn-np:NP1275020.RAljn9oegsWvUnEtjDeDopwON3FcO2E9Q9drNJEOlWRfw130_assertion;
    np:hasProvenance dgn-np:NP1275020.RAljn9oegsWvUnEtjDeDopwON3FcO2E9Q9drNJEOlWRfw130_provenance;
    np:hasPublicationInfo dgn-np:NP1275020.RAljn9oegsWvUnEtjDeDopwON3FcO2E9Q9drNJEOlWRfw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1275020.RAljn9oegsWvUnEtjDeDopwON3FcO2E9Q9drNJEOlWRfw130_assertion a np:Assertion .
  
  dgn-np:NP1275020.RAljn9oegsWvUnEtjDeDopwON3FcO2E9Q9drNJEOlWRfw130_provenance a np:Provenance .
  
  dgn-np:NP1275020.RAljn9oegsWvUnEtjDeDopwON3FcO2E9Q9drNJEOlWRfw130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1275020.RAljn9oegsWvUnEtjDeDopwON3FcO2E9Q9drNJEOlWRfw130_assertion {
  miriam-gene:11235 a ncit:C16612 .
  
  lld:C0036572 a ncit:C7057 .
  
  dgn-gda:DGN550ad7e48de94508a79dc9d7b7076123 sio:SIO_000628 miriam-gene:11235, lld:C0036572;
    a sio:SIO_001121 .
}

dgn-np:NP1275020.RAljn9oegsWvUnEtjDeDopwON3FcO2E9Q9drNJEOlWRfw130_provenance {
  dgn-np:NP1275020.RAljn9oegsWvUnEtjDeDopwON3FcO2E9Q9drNJEOlWRfw130_assertion dcterms:description
      "[Mutations in the essential adaptor proteins CCM2 or CCM3 lead to cerebral cavernous malformations (CCM), vascular lesions that most frequently occur in the brain and are strongly associated with hemorrhagic stroke, seizures, and other neurological disorders.]. 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:25825518;
    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:NP1275020.RAljn9oegsWvUnEtjDeDopwON3FcO2E9Q9drNJEOlWRfw130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:24+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: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" .
}