@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1401656.RAKT_Yc-_iNyjbtRERBTW1JHK6o5RISsgED0cwEgccFMc> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .
dgn-np:NP1401656.RAKT_Yc-_iNyjbtRERBTW1JHK6o5RISsgED0cwEgccFMc130_head {
  this: np:hasAssertion dgn-np:NP1401656.RAKT_Yc-_iNyjbtRERBTW1JHK6o5RISsgED0cwEgccFMc130_assertion ;
    np:hasProvenance dgn-np:NP1401656.RAKT_Yc-_iNyjbtRERBTW1JHK6o5RISsgED0cwEgccFMc130_provenance ;
    np:hasPublicationInfo dgn-np:NP1401656.RAKT_Yc-_iNyjbtRERBTW1JHK6o5RISsgED0cwEgccFMc130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP1401656.RAKT_Yc-_iNyjbtRERBTW1JHK6o5RISsgED0cwEgccFMc130_assertion a np:Assertion .
  dgn-np:NP1401656.RAKT_Yc-_iNyjbtRERBTW1JHK6o5RISsgED0cwEgccFMc130_provenance a np:Provenance .
  dgn-np:NP1401656.RAKT_Yc-_iNyjbtRERBTW1JHK6o5RISsgED0cwEgccFMc130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP1401656.RAKT_Yc-_iNyjbtRERBTW1JHK6o5RISsgED0cwEgccFMc130_assertion {
  miriam-gene:2153 a ncit:C16612 .
  lld:C0524702 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP1401656.RAKT_Yc-_iNyjbtRERBTW1JHK6o5RISsgED0cwEgccFMc130_provenance {
  dgn-np:NP1401656.RAKT_Yc-_iNyjbtRERBTW1JHK6o5RISsgED0cwEgccFMc130_assertion dcterms:description "[Association of a mutation in the coagulation factor V gene (FV Leiden) with deep vein thrombosis and pulmonary thromboembolism has been well documented in the literature, but no study has specifically screened cases of fatal pulmonary thromboembolism for the mutation.]. 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:9700847 ;
    prov:wasDerivedFrom dgn-void:befree-2016 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1401656.RAKT_Yc-_iNyjbtRERBTW1JHK6o5RISsgED0cwEgccFMc130_publicationInfo {
  this: dcterms:created "2016-05-13T12:52:21+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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    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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}