sub:provenance {
  sub:assertion dcterms:description "[Placenta slides of 65 IUFDs with known maternal thrombophilia test results (compound MTHFR C677T and A1298C heterozygosity, n?=?10; MTHFR 677TT homozygosity, n?=?3; protein S deficiency, n?=?0; factor V Leiden mutation, n?=?2; prothrombin gene mutation G20210A, n?=?1; lupus anticoagulant, n?=?2; antiphospholipid syndrome, n?=?1; MTHFR C677T heterozygosity, n?=?5; MTHFR A1298C heterozygosity, n?=?4; and MTHFR 1298CC homozygosity, n?=?2) and of 30 livebirths with positive maternal thrombophilia test results (n?=?5, 2, 0, 9, 2, 0, 2, 7, 2 and 1, respectively, for those thrombophilias) were microscopically examined for septation, fetal vessel thrombosis, intimal fibrin cushions, avascular villi, haemorrhagic endovasculitis and fibromuscular sclerosis.]. 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:22173239 ;
    prov:wasDerivedFrom dgn-void:BEFREE ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:BEFREE pav:importedOn "2017-02-19"^^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 .
}