@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP534126.RAulv7KD2wR4YiQ2XAeaX2M4ygjsqz4xI8cjfRpVA0OQE> .
@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:NP534126.RAulv7KD2wR4YiQ2XAeaX2M4ygjsqz4xI8cjfRpVA0OQE130_head {
  this: np:hasAssertion dgn-np:NP534126.RAulv7KD2wR4YiQ2XAeaX2M4ygjsqz4xI8cjfRpVA0OQE130_assertion;
    np:hasProvenance dgn-np:NP534126.RAulv7KD2wR4YiQ2XAeaX2M4ygjsqz4xI8cjfRpVA0OQE130_provenance;
    np:hasPublicationInfo dgn-np:NP534126.RAulv7KD2wR4YiQ2XAeaX2M4ygjsqz4xI8cjfRpVA0OQE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP534126.RAulv7KD2wR4YiQ2XAeaX2M4ygjsqz4xI8cjfRpVA0OQE130_assertion a np:Assertion .
  
  dgn-np:NP534126.RAulv7KD2wR4YiQ2XAeaX2M4ygjsqz4xI8cjfRpVA0OQE130_provenance a np:Provenance .
  
  dgn-np:NP534126.RAulv7KD2wR4YiQ2XAeaX2M4ygjsqz4xI8cjfRpVA0OQE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP534126.RAulv7KD2wR4YiQ2XAeaX2M4ygjsqz4xI8cjfRpVA0OQE130_assertion {
  miriam-gene:4854 a ncit:C16612 .
  
  lld:C0042373 a ncit:C7057 .
  
  dgn-gda:DGN103f03948eee1aabeab6698a0013ef64 sio:SIO_000628 miriam-gene:4854, lld:C0042373;
    a sio:SIO_001121 .
}

dgn-np:NP534126.RAulv7KD2wR4YiQ2XAeaX2M4ygjsqz4xI8cjfRpVA0OQE130_provenance {
  dgn-np:NP534126.RAulv7KD2wR4YiQ2XAeaX2M4ygjsqz4xI8cjfRpVA0OQE130_assertion dcterms:description
      "[Mutations in the NOTCH1 receptor are associated with several types of cardiac disease and mutations in NOTCH3 cause the dominant adult onset disorder CADASIL (cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy), a vascular disorder with onset in the 4th or 5th decades.]. 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:22306179;
    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:NP534126.RAulv7KD2wR4YiQ2XAeaX2M4ygjsqz4xI8cjfRpVA0OQE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:22+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" .
}