Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1266728.RApXkNfoOP5hYZjU2EGB42xveiRtnAySlkHr84RjpEd2s130_assertion> ?p ?o ?g. }
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- NP1266728.RApXkNfoOP5hYZjU2EGB42xveiRtnAySlkHr84RjpEd2s130_assertion type Assertion NP1266728.RApXkNfoOP5hYZjU2EGB42xveiRtnAySlkHr84RjpEd2s130_head.
- 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.
- NP1266728.RApXkNfoOP5hYZjU2EGB42xveiRtnAySlkHr84RjpEd2s130_assertion evidence source_evidence_literature NP1266728.RApXkNfoOP5hYZjU2EGB42xveiRtnAySlkHr84RjpEd2s130_provenance.
- NP1266728.RApXkNfoOP5hYZjU2EGB42xveiRtnAySlkHr84RjpEd2s130_assertion SIO_000772 25723084 NP1266728.RApXkNfoOP5hYZjU2EGB42xveiRtnAySlkHr84RjpEd2s130_provenance.
- NP1266728.RApXkNfoOP5hYZjU2EGB42xveiRtnAySlkHr84RjpEd2s130_assertion wasDerivedFrom befree-2016 NP1266728.RApXkNfoOP5hYZjU2EGB42xveiRtnAySlkHr84RjpEd2s130_provenance.
- NP1266728.RApXkNfoOP5hYZjU2EGB42xveiRtnAySlkHr84RjpEd2s130_assertion wasGeneratedBy ECO_0000203 NP1266728.RApXkNfoOP5hYZjU2EGB42xveiRtnAySlkHr84RjpEd2s130_provenance.