@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP289634.RA11tgHvbvePMiaRfKuOjhipEONHTcmIm1Rml3B_E5ENs> .
@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:NP289634.RA11tgHvbvePMiaRfKuOjhipEONHTcmIm1Rml3B_E5ENs130_head {
  this: np:hasAssertion dgn-np:NP289634.RA11tgHvbvePMiaRfKuOjhipEONHTcmIm1Rml3B_E5ENs130_assertion ;
    np:hasProvenance dgn-np:NP289634.RA11tgHvbvePMiaRfKuOjhipEONHTcmIm1Rml3B_E5ENs130_provenance ;
    np:hasPublicationInfo dgn-np:NP289634.RA11tgHvbvePMiaRfKuOjhipEONHTcmIm1Rml3B_E5ENs130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP289634.RA11tgHvbvePMiaRfKuOjhipEONHTcmIm1Rml3B_E5ENs130_assertion a np:Assertion .
  dgn-np:NP289634.RA11tgHvbvePMiaRfKuOjhipEONHTcmIm1Rml3B_E5ENs130_provenance a np:Provenance .
  dgn-np:NP289634.RA11tgHvbvePMiaRfKuOjhipEONHTcmIm1Rml3B_E5ENs130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP289634.RA11tgHvbvePMiaRfKuOjhipEONHTcmIm1Rml3B_E5ENs130_assertion {
  miriam-gene:2006 a ncit:C16612 .
  lld:C0042345 a ncit:C7057 .
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    a sio:SIO_001121 .
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dgn-np:NP289634.RA11tgHvbvePMiaRfKuOjhipEONHTcmIm1Rml3B_E5ENs130_provenance {
  dgn-np:NP289634.RA11tgHvbvePMiaRfKuOjhipEONHTcmIm1Rml3B_E5ENs130_assertion dcterms:description "[Our results suggest that the screened cDNA clones are useful disease markers in the genetic diagnosis of primary varicose vein and that the L1 and Alu elements possibly participated in the development of primary varicose veins through their expression patterns in genes encoded with structural proteins, such as collagen, elastin, and tropomyosin.]. 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:15680382 ;
    prov:wasDerivedFrom dgn-void:befree-20140225 ;
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  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 ;
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dgn-np:NP289634.RA11tgHvbvePMiaRfKuOjhipEONHTcmIm1Rml3B_E5ENs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:45+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
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