@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP376016.RA1YlXBalkR3Dl_UMrjlZ6exKQCi9kcy2BE_ZFJJ9W-r4> .
@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:NP376016.RA1YlXBalkR3Dl_UMrjlZ6exKQCi9kcy2BE_ZFJJ9W-r4130_head {
  this: np:hasAssertion dgn-np:NP376016.RA1YlXBalkR3Dl_UMrjlZ6exKQCi9kcy2BE_ZFJJ9W-r4130_assertion ;
    np:hasProvenance dgn-np:NP376016.RA1YlXBalkR3Dl_UMrjlZ6exKQCi9kcy2BE_ZFJJ9W-r4130_provenance ;
    np:hasPublicationInfo dgn-np:NP376016.RA1YlXBalkR3Dl_UMrjlZ6exKQCi9kcy2BE_ZFJJ9W-r4130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP376016.RA1YlXBalkR3Dl_UMrjlZ6exKQCi9kcy2BE_ZFJJ9W-r4130_assertion a np:Assertion .
  dgn-np:NP376016.RA1YlXBalkR3Dl_UMrjlZ6exKQCi9kcy2BE_ZFJJ9W-r4130_provenance a np:Provenance .
  dgn-np:NP376016.RA1YlXBalkR3Dl_UMrjlZ6exKQCi9kcy2BE_ZFJJ9W-r4130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP376016.RA1YlXBalkR3Dl_UMrjlZ6exKQCi9kcy2BE_ZFJJ9W-r4130_assertion {
  miriam-gene:5054 a ncit:C16612 .
  lld:C0162871 a ncit:C7057 .
  dgn-gda:DGNafa3d9a401abc9c884a23c4957e289e1 sio:SIO_000628 miriam-gene:5054 , lld:C0162871 ;
    a sio:SIO_001121 .
}
dgn-np:NP376016.RA1YlXBalkR3Dl_UMrjlZ6exKQCi9kcy2BE_ZFJJ9W-r4130_provenance {
  dgn-np:NP376016.RA1YlXBalkR3Dl_UMrjlZ6exKQCi9kcy2BE_ZFJJ9W-r4130_assertion dcterms:description "[The magnitude of this effect, which refers to the AAA patients unselected for familial occurrence, indicates that the disturbance of aortic wall physiology caused by the presence of the MTHFR 677T allele is greater than the effect of the earlier described allele disequilibrium at the polymorphic alleles of the PAI1 (plasminogen activator inhibitor 1) gene seen only in familial cases of AAA.]. 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:12590185 ;
    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:NP376016.RA1YlXBalkR3Dl_UMrjlZ6exKQCi9kcy2BE_ZFJJ9W-r4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:40+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" .
}