@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP556048.RAx2mZL5zS2eW0btEk1aSho90YYjWgdboB9766zS6J1CI> .
@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:NP556048.RAx2mZL5zS2eW0btEk1aSho90YYjWgdboB9766zS6J1CI130_head {
   this: np:hasAssertion dgn-np:NP556048.RAx2mZL5zS2eW0btEk1aSho90YYjWgdboB9766zS6J1CI130_assertion ;
    np:hasProvenance dgn-np:NP556048.RAx2mZL5zS2eW0btEk1aSho90YYjWgdboB9766zS6J1CI130_provenance ;
    np:hasPublicationInfo dgn-np:NP556048.RAx2mZL5zS2eW0btEk1aSho90YYjWgdboB9766zS6J1CI130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP556048.RAx2mZL5zS2eW0btEk1aSho90YYjWgdboB9766zS6J1CI130_assertion a np:Assertion .
  dgn-np:NP556048.RAx2mZL5zS2eW0btEk1aSho90YYjWgdboB9766zS6J1CI130_provenance a np:Provenance .
  dgn-np:NP556048.RAx2mZL5zS2eW0btEk1aSho90YYjWgdboB9766zS6J1CI130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP556048.RAx2mZL5zS2eW0btEk1aSho90YYjWgdboB9766zS6J1CI130_assertion {
   miriam-gene:4524 a ncit:C16612 .
  lld:C0398623 a ncit:C7057 .
  dgn-gda:DGNa6db68df64b9eefbd0dc9ddf9ebc9c19 sio:SIO_000628 miriam-gene:4524 , lld:C0398623 ;
    a sio:SIO_001122 .
}
dgn-np:NP556048.RAx2mZL5zS2eW0btEk1aSho90YYjWgdboB9766zS6J1CI130_provenance {
   dgn-np:NP556048.RAx2mZL5zS2eW0btEk1aSho90YYjWgdboB9766zS6J1CI130_assertion dcterms:description "[Based on the hypothesis that an inherited predilection to hypercoagulability may predispose to HSP or may mark those who develop acute clinical manifestations, we evaluated the possible roles of methylenetetrahydrofolate reductase (MTHFR) gene C677T, factor V (FV) gene G1691A (Leiden), and prothrombin gene G20210A polymorphisms in patients with HSP.]. 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:16791607 ;
    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:NP556048.RAx2mZL5zS2eW0btEk1aSho90YYjWgdboB9766zS6J1CI130_publicationInfo {
   this: dcterms:created "2016-05-13T12:45:56+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:disgenetv3.0rdf ;
    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 "v4.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}