@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1275019.RAaVw_KIOdXo2tr63cHlBTb_B1Xs5JZj0bh5u5YVTIBs8> .
@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:NP1275019.RAaVw_KIOdXo2tr63cHlBTb_B1Xs5JZj0bh5u5YVTIBs8130_head {
  this: np:hasAssertion dgn-np:NP1275019.RAaVw_KIOdXo2tr63cHlBTb_B1Xs5JZj0bh5u5YVTIBs8130_assertion;
    np:hasProvenance dgn-np:NP1275019.RAaVw_KIOdXo2tr63cHlBTb_B1Xs5JZj0bh5u5YVTIBs8130_provenance;
    np:hasPublicationInfo dgn-np:NP1275019.RAaVw_KIOdXo2tr63cHlBTb_B1Xs5JZj0bh5u5YVTIBs8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1275019.RAaVw_KIOdXo2tr63cHlBTb_B1Xs5JZj0bh5u5YVTIBs8130_assertion a np:Assertion .
  
  dgn-np:NP1275019.RAaVw_KIOdXo2tr63cHlBTb_B1Xs5JZj0bh5u5YVTIBs8130_provenance a np:Provenance .
  
  dgn-np:NP1275019.RAaVw_KIOdXo2tr63cHlBTb_B1Xs5JZj0bh5u5YVTIBs8130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1275019.RAaVw_KIOdXo2tr63cHlBTb_B1Xs5JZj0bh5u5YVTIBs8130_assertion {
  miriam-gene:11235 a ncit:C16612 .
  
  lld:C2919945 a ncit:C7057 .
  
  dgn-gda:DGN7cb426ad9221c9202c14e8029b501dff sio:SIO_000628 miriam-gene:11235, lld:C2919945;
    a sio:SIO_001121 .
}

dgn-np:NP1275019.RAaVw_KIOdXo2tr63cHlBTb_B1Xs5JZj0bh5u5YVTIBs8130_provenance {
  dgn-np:NP1275019.RAaVw_KIOdXo2tr63cHlBTb_B1Xs5JZj0bh5u5YVTIBs8130_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:NP1275019.RAaVw_KIOdXo2tr63cHlBTb_B1Xs5JZj0bh5u5YVTIBs8130_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" .
}