Matches in Nanopublications for { ?s ?p "[Hereditary hypofibrinolysis, which is mediated by 4G/4G homozygosity for the PAI-1 gene, is an independent risk factor for pregnancy complications, probably acting through thrombotic induction of placental insufficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 1 of
1
with 100 items per page.
- NP1266728.RApXkNfoOP5hYZjU2EGB42xveiRtnAySlkHr84RjpEd2s130_assertion description "[Hereditary hypofibrinolysis, which is mediated by 4G/4G homozygosity for the PAI-1 gene, is an independent risk factor for pregnancy complications, probably acting through thrombotic induction of placental insufficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1266728.RApXkNfoOP5hYZjU2EGB42xveiRtnAySlkHr84RjpEd2s130_provenance.