@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP822740.RAnM1XWgAeplc10nd56v3VpJc0-XFITp1hHRDQuqawtTQ> .
@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:NP822740.RAnM1XWgAeplc10nd56v3VpJc0-XFITp1hHRDQuqawtTQ130_head {
  this: np:hasAssertion dgn-np:NP822740.RAnM1XWgAeplc10nd56v3VpJc0-XFITp1hHRDQuqawtTQ130_assertion;
    np:hasProvenance dgn-np:NP822740.RAnM1XWgAeplc10nd56v3VpJc0-XFITp1hHRDQuqawtTQ130_provenance;
    np:hasPublicationInfo dgn-np:NP822740.RAnM1XWgAeplc10nd56v3VpJc0-XFITp1hHRDQuqawtTQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP822740.RAnM1XWgAeplc10nd56v3VpJc0-XFITp1hHRDQuqawtTQ130_assertion a np:Assertion .
  
  dgn-np:NP822740.RAnM1XWgAeplc10nd56v3VpJc0-XFITp1hHRDQuqawtTQ130_provenance a np:Provenance .
  
  dgn-np:NP822740.RAnM1XWgAeplc10nd56v3VpJc0-XFITp1hHRDQuqawtTQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP822740.RAnM1XWgAeplc10nd56v3VpJc0-XFITp1hHRDQuqawtTQ130_assertion {
  miriam-gene:11235 a ncit:C16612 .
  
  lld:C2919945 a ncit:C7057 .
  
  dgn-gda:DGNe67a22216305a7977cdbafe2172311ce sio:SIO_000628 miriam-gene:11235, lld:C2919945;
    a sio:SIO_001122 .
}

dgn-np:NP822740.RAnM1XWgAeplc10nd56v3VpJc0-XFITp1hHRDQuqawtTQ130_provenance {
  dgn-np:NP822740.RAnM1XWgAeplc10nd56v3VpJc0-XFITp1hHRDQuqawtTQ130_assertion dcterms:description
      "[Here we have shown in zebrafish that expression of mutant ccm3 proteins (ccm3Delta) known to cause cerebral cavernous malformation in humans confers cardiovascular phenotypes identical to those associated with loss of ccm1 and ccm2.]. 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:20592472;
    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:NP822740.RAnM1XWgAeplc10nd56v3VpJc0-XFITp1hHRDQuqawtTQ130_publicationInfo {
  this: dcterms:created "2016-05-13T12:47:57+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" .
}