@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP789053.RA5QxuRhbdCfjhfyOmPH7TM7axCtnvHxTtxsAfphkvijQ> .
@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:NP789053.RA5QxuRhbdCfjhfyOmPH7TM7axCtnvHxTtxsAfphkvijQ130_head {
  this: np:hasAssertion dgn-np:NP789053.RA5QxuRhbdCfjhfyOmPH7TM7axCtnvHxTtxsAfphkvijQ130_assertion ;
    np:hasProvenance dgn-np:NP789053.RA5QxuRhbdCfjhfyOmPH7TM7axCtnvHxTtxsAfphkvijQ130_provenance ;
    np:hasPublicationInfo dgn-np:NP789053.RA5QxuRhbdCfjhfyOmPH7TM7axCtnvHxTtxsAfphkvijQ130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP789053.RA5QxuRhbdCfjhfyOmPH7TM7axCtnvHxTtxsAfphkvijQ130_assertion a np:Assertion .
  dgn-np:NP789053.RA5QxuRhbdCfjhfyOmPH7TM7axCtnvHxTtxsAfphkvijQ130_provenance a np:Provenance .
  dgn-np:NP789053.RA5QxuRhbdCfjhfyOmPH7TM7axCtnvHxTtxsAfphkvijQ130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP789053.RA5QxuRhbdCfjhfyOmPH7TM7axCtnvHxTtxsAfphkvijQ130_assertion {
  miriam-gene:1281 a ncit:C16612 .
  lld:C0019247 a ncit:C7057 .
  dgn-gda:DGN96a4f2c0c4057f45ddaa0dde82dc2cf5 sio:SIO_000628 miriam-gene:1281 , lld:C0019247 ;
    a sio:SIO_001121 .
}
dgn-np:NP789053.RA5QxuRhbdCfjhfyOmPH7TM7axCtnvHxTtxsAfphkvijQ130_provenance {
  dgn-np:NP789053.RA5QxuRhbdCfjhfyOmPH7TM7axCtnvHxTtxsAfphkvijQ130_assertion dcterms:description "[Experiments were carried out to test the hypothesis that familial aortic aneurysms, either thoracic or abdominal, are caused by mutations in the gene for type III procollagen (COL3A1) similar to mutations in the same gene that have been shown to cause rupture of aorta and other disastrous consequences in the rare genetic disorder known as Ehlers-Danlos syndrome type IV.]. 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:2243125 ;
    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:NP789053.RA5QxuRhbdCfjhfyOmPH7TM7axCtnvHxTtxsAfphkvijQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:01+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" .
}