@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP61290.RAog2hLXkbQ7MMM58VbS5MvRatUBZU6wQJ-BG1KoSWrxg> .
@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:NP61290.RAog2hLXkbQ7MMM58VbS5MvRatUBZU6wQJ-BG1KoSWrxg130_head {
  this: np:hasAssertion dgn-np:NP61290.RAog2hLXkbQ7MMM58VbS5MvRatUBZU6wQJ-BG1KoSWrxg130_assertion ;
    np:hasProvenance dgn-np:NP61290.RAog2hLXkbQ7MMM58VbS5MvRatUBZU6wQJ-BG1KoSWrxg130_provenance ;
    np:hasPublicationInfo dgn-np:NP61290.RAog2hLXkbQ7MMM58VbS5MvRatUBZU6wQJ-BG1KoSWrxg130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP61290.RAog2hLXkbQ7MMM58VbS5MvRatUBZU6wQJ-BG1KoSWrxg130_assertion a np:Assertion .
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  dgn-np:NP61290.RAog2hLXkbQ7MMM58VbS5MvRatUBZU6wQJ-BG1KoSWrxg130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP61290.RAog2hLXkbQ7MMM58VbS5MvRatUBZU6wQJ-BG1KoSWrxg130_assertion {
  miriam-gene:4524 a ncit:C16612 .
  lld:C0042487 a ncit:C7057 .
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    a sio:SIO_001122 .
}
dgn-np:NP61290.RAog2hLXkbQ7MMM58VbS5MvRatUBZU6wQJ-BG1KoSWrxg130_provenance {
  dgn-np:NP61290.RAog2hLXkbQ7MMM58VbS5MvRatUBZU6wQJ-BG1KoSWrxg130_assertion dcterms:description "[ The findings of this study illustrate the power of ANN in evaluating multifactorial data, and show that the different sensitivities of the models of elaboration are related to the characteristics of the data. This may contribute to a better understanding of the role played by genetic polymorphisms in VTE, and help to define, if possible, a test panel of genetic variants to estimate an individual's probability of developing the disease.]. 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:16266408 ;
    prov:wasDerivedFrom dgn-void:gad-20130706 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP61290.RAog2hLXkbQ7MMM58VbS5MvRatUBZU6wQJ-BG1KoSWrxg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:29+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> ;
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    pav:version "v2.1.0.0" .
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